TW201247697A - Isoxazolidine derivatives - Google Patents
Isoxazolidine derivatives Download PDFInfo
- Publication number
- TW201247697A TW201247697A TW101108588A TW101108588A TW201247697A TW 201247697 A TW201247697 A TW 201247697A TW 101108588 A TW101108588 A TW 101108588A TW 101108588 A TW101108588 A TW 101108588A TW 201247697 A TW201247697 A TW 201247697A
- Authority
- TW
- Taiwan
- Prior art keywords
- phenanthrene
- hydroxy
- difluoro
- dimercapto
- pentylene
- Prior art date
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- 125000000217 alkyl group Chemical group 0.000 claims description 47
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 40
- 125000003118 aryl group Chemical group 0.000 claims description 34
- 150000003839 salts Chemical class 0.000 claims description 33
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0036—Nitrogen-containing hetero ring
- C07J71/0057—Nitrogen and oxygen
- C07J71/0068—Nitrogen and oxygen at position 16(17)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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Description
201247697 六、發明說明: 【發明所屬之技術領域】 本發明係有關於新穎糖皮質激素系列之抗發炎及抗過敏 化合物,此等化合物之製備方法,含有此等化合物之醫藥 組成物’其組合物及其治療用途。更明確言之,本發明係 關於屬於異》号唾α定衍生物之糖皮質激素。 【先前技術】 皮質類固醇乃強力抗發炎劑,可減少發炎細胞的數目、 活性、及移動。 皮質類固醇常用於治療寬廣範圍之慢性及急性發炎病 況,包括氣喘、慢性阻塞性肺病(c〇PD)、過敏性鼻炎、類 風濕性關節炎、發炎性腸病、及自體免疫病。 皮質類固醇係透過糖皮質激素受體(GR)而媒介其功效。 皮質類固醇結合至GR而誘生其核轉位,核轉位又轉而透過 DNA結合㈣峨例如轉活化)_ &dna結合非依賴型(例 如轉抑制)機轉而影響多個下游路徑。 用於治療肺臟慢性發炎病況之皮質類固醇諸如氣喘及 C〇PD目前係經由吸入投藥。採用吸入型皮質類固醇(ICS) 之優點之-為可能直接遞送藥物於作用部位,限制系统性 副作用’如此導致更快速臨歧歧更高治療比。 雖然.治療可提供重大療效,特別個於氣喘, 地係最小化咖祕暴露,ICS㈣屬暴露可能導致與 101108588 201247697 慢性長期投藥相聯結的非期望負φ效應的出;見及嚴重程 度。此外’目前於臨床實務上使用的ICS之作用持續時間有 限,促成對疾病的管理並非最佳。雖然吸入劑技術乃目標 鎖定肺臟的關鍵重點,在皮質類固醇分子骨架上的取代基 之調控對藥力學性質及藥效學性質的最佳化相當重要,俾 便減低經口生物利用率,侷限藥理活性只限於肺(前驅藥及 軟性藥),及提高系統清除率。此外,ICS在肺臟的長期持續 活性乃高度期望’原因在於每日投藥ICS —次將允許減少投 藥頻率,及因而實質上改進病人對醫囑的遵從性,及結果 導致疾病管理與控制上的改善。總結而言,迫切醫療需求 需要發展具有改良藥力學特性及藥效學特性的ICS。
糖皮質激素異°号唑啶衍生物例如係說明於WO 2006/005611、GB 1578446及說明於「Synthesis and topical anti-inflammatory activity of some steroidal [16α,17a-d] isoxazolidines」(J. Med. Chem.,25, 1492-1495, 1982)。 數種糖皮質激素異崎唑啶衍生物也係敘述於共同審查中 之專利申請案WO 2011/029547。 出乎意外地發現本發明化合物顯示改良發展性,改良藥 力學特性或藥效學特性,諸如系統性暴露、作用選擇性、 作用強度、及作用持續時間。 【發明内容】 本發明係有關於糖皮質激素系列之抗發炎及抗過敏化合 101108S88 4 201247697 物’此等化合物之製備方法’含有此等化合物之組成物, 其治療用途及其與其它用於治療呼吸病症的醫藥上活性成 分之組合物’該等活性成分包括p2_促效劑、抗簟毒驗劑、 皮質類固醇、有絲分裂原活化蛋白質激酶(P38 MAP激酶) 抑制劑、核因子K_B激酶亞單元β(ΐΚΚ2)抑制劑、人類嗜中 性細胞彈性蛋白酶(ΗΝΕ)抑制劑、磷酸二酯酶4(PDE4)抑制 劑、白二烯調節劑、非類固醇抗發炎劑(NSAID)、及黏液調 節劑。 【實施方式】 更明確言之,本發明係有關於通式(I)化合物
其中
Ri 為_(CH2VZ-(CH2)n,_R3,其中n及 η’各自獨立地為0、1 或2 ; ζ為單鍵或係選自於-S-、-0-及-〇C(R4R5)-; R3係選自於由下列所組成之組群: _H、_ 原子、CN、〇H、CONH2、(C「C6)炫基、(C2-C4) 1〇Π〇8588 5 201247697 稀基(CrC6)函烧基、(C2')炔基、及(cvc6)院基確醯基 及(Ci_C0)烷基甲醯基; •NR4R5,其中R4及立地選自於由(Cl_C6)烧基及 (Ci-C6)燒氧基所組成之組群· -(㈣)環院基、(%)雜環院基、芳基及雜芳基其各 自係選擇n地經以-或多個自原子或側氧基或⑶基取代; 及 R2係選自於由下列所組成之組群: 線生或分支(CrC8)貌基、(CrC6)^氧基、(Ci_c6)函烧基, 選擇性地經以-或多個CN基或⑽子取代; _(CH2)mR6,其中r0係選自於由下列所組成之組群: (CrC8)環烷基、(c^C8)雜環烷基、芳基、(Ci_C6)芳基烷基、 芳基氧基、芳基硫基、及雜芳基,其各自係選擇性地經以 選自於由下列所組成之組群中之—或多個取代基取代:侧 氧基、OH、i 原子、CN、NH2、CONH2、N〇2、NHC(0)H、 線性或分支(crc:6)烷基、線性或分支(CrC6)鹵烷基、線性 或分支(eve:6)烷氧基、線性或分支(CrC6)函烷氧基、(CrC6) %基烧氧基、(CrC6)齒烷氧基、(Crc6)烷氧基曱醯基、(Crc6) 燒基叛基、(crc6)烷基磺醯基及(CrC6)烷基磺烷基、(Crc6) 炫*氧基續酿基、(Ci-C6)齒烷基磺醯氧基、胺基磺醯基、(c3-c8) 環烧基、(CrC6)雜環烷基及雜芳基,其中m為0或1至3之整 數及 101108588 6 201247697 X及Y獨立地為Η或鹵原子,及 其醫藥上可接受之鹽, 但限制條件為當Ri為_CH2〇H基及r2為(Cl_C6)烷基或 (CrC8)環烷基時,X及γ為氟原子。 於本說明中除非另行載明,否則「鹵原子」一詞包括氟、 氣、溴、及碘原子。 表示法「線性」及「直鏈」具有相同定義。 「(Crc6)烷基」、「(crc8)烷基」、或「(Crc15)烷基」等詞 係指直鏈或分支鏈烷基其中碳原子數分別為1至6、1至8、 或1至15。該等基團之實例為曱基、乙基、正丙基、異丙基、 正丁基、異丁基、第二丁基、第三丁基、戊基、己基、庚 基、辛基、乙基-丁基、丙基-丁基、曱基-丁基、乙基_甲基-丙基、十六烧基等。 表示法「(C2_C6)烯基」係指含有一或多個雙鍵之直鏈或 分支碳鏈,其中碳原子數為2至6。該等基團之實例包括乙 烯基、丙烯基、丁烯基、戊烯基、己烯基等。 表示法「(C2-C6)炔基」係指含有一或多個參鍵之直鏈或 分支碳鏈’其中碳原子數為1至6。該等基團之實例包括乙 炔基、丙炔基、丁炔基、戊炔基、己炔基等。 表示法「(CrC6)烧基羧基」係指烷基-c〇〇基。 「(CrC6)烷氧基」一詞係指烷基-氧基(例如烷氧基),烷 基部分係如前述定義。該等基團之實例如此包含曱氧基、 101108588 7 201247697 乙氧基、正丙氧基、異丙氧基、正丁氧基、異丁氧基、第 二丁氧基、第三丁氧基、戊氧基、己氧基等。 表示法「(CrC6)烷氧基曱醯基」及「(crc0)羥基烷氧基」 分別係指烷氧基-CO-基及(OH)烷氧基。 表示法「(CrC6)齒烷基」及「(CrC6)鹵烷氧基」係指前 述「(CrC6)烷基」及「(CrC6)烷氧基」,其中一或多個氫原 子係由可彼此相同或相異之一或多個鹵原子所置換。 如此該等(CrC6)齒烷基及(Crc0)函烷氧基之實例包括鹵 化、多_化及全函化烧基及烧氧基其中全部氫原子係由4 原子所置換,例如三氟曱基或三氟曱氡基。 表示法「(C^-Cs)環烧基」係指含3至8個碳原子之一環戋 二環脂肪族烴基。實例包括環丙基、環丁基、環戊基、環 己基、環庚基、二環[2.2.1]庚-2-基等。 表示法「(c3-c8)雜環烧基」係指((VC8)環燒基,i中至 少一個環碳原子係以雜原子或雜芳香族基(例如N、謝、S 或〇)所置換。 較佳為6至15個 環系或二環系或 表不法「芳基」係指含6至20個環原子, 環原子’及其中至少_個環為芳香環之一 三環系。 又以芳基取代之(CrC6) 表示法「(CrC6)芳基烷基」係指 烷基。 分別係指芳基_氧基 表不法「芳基氧基」及「芳基硫基」 101108588 201247697 及芳基-S-基,芳基部分係如前文定義。 表示法「(CVQ)烧基硫院基」及「(Cl_C6)燒基續酿基」 分別係指烷基-S-基及烷基_S〇2_基。 土 「(CVCO函烷基磺醯基氧基」一詞係指_烷基 基。 表示法「胺基磺醯基」係指nh2s(o2)-。 二==基」係指含5至2_原子,較佳5至_ :環二環系’其中至少-個環為芳 Ν、ΝΗ、S或〇)。&子為雜原子或雜芳香族基(例如 適當芳基或雜芳美_ 口各、口比。坐、呼伞土 實例包括例如嗟吩、苯、口比 水唑、里《吔 味吐唆、料基團等。…異麵、嗟峻“比咬、 適备芳基或雜芳武 a 喋咬、笨并三嗅ϋ、之貫例包括萘、聯苯、嗓呤、 吩、二輕苯二二琳、異啥琳、。«、異十朵、苯并嗟 基團等。 ' 、一氫苯并二呤呼、噻唑、苯并哼畊
適當芳基或雜劣I 基二環系之笨并狗合;^之實例包㈣基以及前述雜芳 表不法「綠性」及「直鏈」恩七 熟諳技藝人 恁」具有相同定義。 朴、5、知、牝、::然〗:知:式(ί)化合物至少於位置如、 101108588 5有非對稱中心,因此可以 201247697 許多光學立體異構物及其混合物形式存在。 因此本發明也係有關於全部此等形式及其混合物。 較佳化合物為通式⑴化合物其中立體異構源碳原子之立 體化學係報告於下式(Γ),絕對組態係以康英格沛洛 (Cahn-Ingold-Prelog)命名為基礎基於各基團的優先順序分 配
及其中R!及R_2之意義係如前文定義。 於一個較佳具體例中,針對式(Γ)化合物,於非對稱中心 4a之絕對組態為(S),於4b為(R),於5為(8),於6&為(8),於 6b為(R)’於9a為(S),於i〇a為⑻,於1〇b為⑻,及於12為(3)。 通式⑴化合物特別係與醫藥上可接受之酸可形成酸加成 鹽。 如此式(I)化合物之醫藥上可接受之酸加成鹽也涵蓋式(1,) 之醫藥上可接受之酸加成鹽’包括與無機酸例如氫齒酸諸 如氫氟酸、氫氣酸、氫溴酸或氫峨酸;硝酸、硫酸、填酸; 及有機酸,例如脂肪族一羧酸諸如曱酸、乙酸、三氟乙酸 101108388 201247697 =丙U日肪㈣基酸諸如乳酸、檸檬酸、 如心烯二酸、反丁烯二酸、草酸二:果 ^ 本甲駄’方香族羥基酸及磺醆所形成之# 樂上可接受之醆加成鹽。 ㈣成之4 此等鹽類可ϋ α t 備。 9 D鹽形成程序從式(1)或(I,)化合物製 ;較佳具體例中,於本發明之化合物中,X及Y中之至少 一者為㈣子’ m為零及R6為選擇性地經取代之芳基、 (C3咖燒基或雜芳基。於更佳具體财,X及Y皆獨1地 為i原子’及m為零,及&為選擇性地經取代之芳基、(q-Cs) 祕基或雜芳基。於又更佳具體例中,X及Y皆為氟,及m 為零’及116為選擇㈣經取代之絲、(CrC趣烧基或雜 芳基。 於較佳具體例中,於本發明之化合物中,m為零,r6為選 擇性地經取代之芳基、(CrCs)環烷基或雜芳基,心為 -(CH2)n-Z-(CH2)n,-R3,其中n為卜Z為單鍵,n,為〇及化為 -OH ;或R丨為_(cH2)n-Z-(CH2)n,-R3 ’ 其中η為0,Z為-S-,η, 為1及尺3為鹵原子;或111為-(〇12)1^-((:112)11,-1^,其中11為〇, Ζ為鍵結’ η’為1及]^係選自於由鹵原子、CN、CONH2、(CrC6) 鹵烷基及(CVCd烷基甲醯基所組成之組群。於更佳具體例 中,Ri 為-(CH2)n-Z-(CH2)n,-R3 ’ 其中 η為 0,Z為-S-,η’為 1 及尺3為鹵原子;或以1為-((^2)11_乙-(〇112)11,-113,其中11為0,2 101108588 201247697 為鍵結5 η ’為1及R3為鹵原子。 於較佳具體例中,於本發明化合物中,R!係選自於由下 列基團所組成之組群:曱基、羥基、羥基甲基、Ν-曱氧基-Ν-曱基胺基、Ν-曱基-Ν-氰基曱基、氣曱基、氟曱基、氟曱氧 基、氟乙氧基、氯曱氧基、氰基曱基、甲基硫烷基、曱基 硫烷基曱基、環丙基曱氧基、氟乙基硫烷基、三氟乙基硫 烷基、環丁基硫烷基、氰基曱氧基及下式(h)、(h’)、(h’”)、 (i)、(i’)、(1)、(1,)、(1”)或(1”’)之基團
(h,”) (i,) 於較佳具體例中,於本發明化合物中,R2係選自於由下 列基團所組成之組群:環己基、乙基-丁基、苯基-丙基、苯 氧基-乙基、胺基-曱醯基-苯基、胺基-磺醯基-苯基、溴-苯 基、氰基-苯基、環丙基-苯基、曱氧基·•节基、丙基-丁基、 曱基-丁基、第三丁基-苄基、曱基-苄基、二氣-苯基、氣-°夫°南-2-基-曱基、氯塞吩-2-基·•曱基、苯基硫烧基-乙基、環 101108588 12 201247697 己基、環戊基甲基、乙基-2-曱基-丙基、4-氣-3·三氟曱基-笨基、4-氣-3 -曱基-苯基、三氟-丙基、3,3-二甲基-丁基、氟 -苄基、嘆吩-2-基f基、咬喃-2-基曱基、乙基-甲基_丙基、 乙基-丁基、甲氧基-曱酿基-苯基、曱氧基-甲醯基_节基、環 己基曱基、%•己基本基、甲基硫烧基-节基、曱基硫院基。塞 吩基、第二丁基、環戊基曱基、第三丁氧基_苄基、第三丁 氧基-甲疏基-苄基、吼。定、。塞唾_4_基、嗔唾_2_基曱基、$ 。坐-2-基、咪唑-1-基-乙基、環己基_乙基、吡啶_3基_丙基、 呋喃-3-基、1H-吲哚-3-基甲基、1-甲基-iH_吲哚_3_基曱基、 喹啉-7-基曱基、苯并噻唑-2-基曱基、二環[22 1:}庚_2_基、 丙基苄基、喹啉-5-基甲基、苯并呋喃_3_基、苯并[i,3]二哼 呃-5-基、曱基_ιΗ_吲哚_2•基、曱基_1]9>引哚_3_基曱基、甲 基-磺醯基-苯基、曱基-1H-咪唑基曱基、1H-咪唑-2-基曱 基、氣-苯基、甲笨基、氣_苄基、羥基_苄基、噻吩_2_基甲 基、呋喃-2-基曱基、甲基-苄基、甲氧基_苄基、丁氧基-苄 基、環戊基曱基、氯-噻吩_2_基曱基、曱基_噻吩_2_基_曱基、 一%庚基、咪唑基乙基、4-哌啶_4_基_曱基_苯基及下式⑴、 (t’)、(t”)或(t’,,)基團 -〇-〇,8χ -〇-μλη -~〇^〇/SncF3 ‘ (t) (〇 (t”) (t”,) 較佳通式(I)或(r)化合物具有式(IA),其中X&Y為氟原 101108588 13 201247697 子,η為〇或1,n’為〇或i ; z為單鍵,或係選自-s_、_〇·及 -〇C(r4r5) ; r3係選自於由H、齒原子、、 -NR4R5 > (CrC6)^& , (C2-C4)^^ ^ (C2-C4)^^ ' (CrC6) 烧基崎醯基、(crc6)燒基曱醯基及選擇性地經取代之一環 (CrQ)雜環烷基所組成之組群;及^、I、基團係如前 文針對式(I)化合物之定義。 其它較佳式(I)或(Γ)化合物具有式(IB),其中乂及丫為氟,
Ri為-(CH2)n-Z_(CH2)n,-R3,其中 n為卜 2為單鍵,η,為^R3 為-OH ;及R2基係如前文對式⑴化合物之定義。 較佳通式(I)或(Γ)化合物具有式(IC),其中父及¥為氟、m 為零及R6為選擇性地經取代之絲或雜絲,使得&表示 選擇性經取代之絲或雜綠H係如前文式⑴化合物 之定義。 於一較佳具體例中,於式(1C)化合物中,R2為選擇性地經 取代之苯基。 於另一較佳具體例中,於式(IC)化合物中,R2為選擇性地 經取代之雜芳基。 依據本案所述類似程序及方法,可獲得下列式(Ic)化合 物: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二亂 _5· 羥基-4a,6a·二曱基_2_側氧基·8_吡啶_3基 -2,4&,41),5,6,6&,8,9,93,10,1〇3,1〇13,11,12-十四氫-7-«号-8“丫-戊 101108588 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S·氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-噻唑-4-基 -2,4\415,5,6,6\8,9,9&,10,1〇3,101),11,12-十四氫-7-'1等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二甲基-8- σ等〇坐-2-基-2-側氧基 -2,4&,41),5,6,618,9,93,10,10&,101),11,12-十四氫-7-«等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-8-夫喃-3-基-5-經基-4a,6a-二曱基-2-側氧基 -2,4\仆,5,6,618,9,9&,10,1(^,1015,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_8-苯并呋喃-3-基-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基 -2,4\413,5,6,6&,8,9,9&,10,10\101),11,12-十四氫-7-崎-8,吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS510aS,10bS,12S)-8-苯并[1,3]二 呢·5-基-4b,12-二氣·5-經基-4a,6a·二曱基_2-侧氧基 -2,4&,415,5,6,6&,8,9,9&,10,10攻,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 101108388 15 201247697 羥基-4a,6a-二甲基-8-(1-曱基-1H-吲哚-2-基)-2-側氧基 -2,4&,41?,5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-»号,8-。丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4&,413,5,6,618,9,93,10,1(^,101),11,12-十四氫-7-崎,8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 羥基-4a,6a-二曱基-2-側氧基-8-對-甲苯基 -2,4\41),5,6,618,9,9&,10,10&,101?,11,12-十四氫-73等-8-吖-戊 搭烯并[2,1-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-8-(4-曱氧基-苄基)-4a,6a-二曱基-2-侧氧基 -2,4&,41),5,6,6&,8,9,93,10,1(^,1015,11,12-十四氫-7-崎-8,吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 羥基-4a,6a-二曱基-2-側氧基-8-鄰曱苯基 -2,4&,41),5,6,63,8,9,9&,10,1(^,101),11,12-十四氫-7_〇等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3·氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4&,41?,5,6,63,8,9,9&,10,10&,101),11,12-十四氫-7-崎-8-吖-戊 10110858S 16 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 羥基-4a,6a-二曱基-2-側氧基-8-間-甲苯基 -2,4&,41),5,6,6&,8,9,9\10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 羥基-8·(3-曱氧基·苯基)_4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-4各〇丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯。 於較佳具體例中,本發明係有關於通式(ID)化合物
(ID) 其中
Ri為-(CH2)n-Z-(CH2)n,-R3,其中η及n,各自獨立地為0、1 或2 ; Ζ為單鍵或係選自於-S-及-0-; I係選自於由下列所組成之組群: _Η、_原子、CN、CONH2、ΟΗ、直鏈或分支(CrC15)烧 基、(CrC6)s烷基及(CrC6)烷基磺醯基; 101108588 17 201247697 -NR^5 ’其中I及Rs獨立地係選自於由(CiCj烷基及 (CrC6)烧氧基所組成之組群; -(CrC8)環烷基、(CrC8)雜環烷基、芳基及雜芳基其各 自選擇性地經以一或多個_原子或側氧基取代; R2係選自於由下列所組成之組群: -直鏈或分支(CrC8)烷基; --(CHiR6,其中^為%%)環烷基,其中 之整數及 其醫藥上可接受之鹽。 式(ID)化合物之實例包括: (4汪8,仆11,58,6&8,6511,938,1(^,1(^8,128)-8-環戊基甲基 -4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,扑,5,6,63,8,9,9\10,10&,101),11,12-十四氫-7-4-8-。丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12·二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4狂,41),5,6,6\61),8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 •4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 2,4&,41>,5,6如,8,9,93,10,1(^,101),11,12-十四氫-7-碍-8-。丫-戍 搭烯并[2,l-a]菲-6b·硫代羧酸S-氟曱基酯。 101108S88 18 201247697 依據本案所述類似程序及方法,可獲得下列式(ID)化合 物: (4&8,扑11,58,6&3,沾11,9&3,1(^3,1(^8,128)-8-(2-環己基-乙 基)_4b,12·二敗-5-經基-4a,6a-二曱基-2-側氧基 -2,4日,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7“号-8-吖-戊 搭稀并[2,l-a]菲-6b-硫代緩酸S-氣曱基醋; (4&8,仆11,58,633讲11,9&8,10&8,1(^8,128)-8-二環[2.2.1]庚 -2-基-4b,12- 一乱-5-經基-4a,6a·二曱基-2-側氧基 2,4\413,5,6加,8,9,9&,1〇,1〇&,1〇1?,11,12-十四氣-7-»等-8-吖-戊 搭烯并[2,1-a]菲-6b-硫代幾酸S-氟甲基酯。 於更佳化合物中,本發明係有關於通式(IE)化合物
(IE) 其中
Ri為(CH2)n-Z-(CH2)n,-R3,其中n及n,各自獨立地為〇、! 或2 ; Z為單鍵或係選自於-s_及·〇_ ; R3係選自於由下列所組成之組群: 101108588 201247697 -Η、齒原子、CN、OH、(CrC6)烧基、(C「C6)i!烷基及(Ci_c 烧基確酿基; -NH,其中I及Rs獨立地係選自於由^烷義 (Ci-C6)烧氧基所組成之組群; -(Ci-C6)烧基; •(CrC8)環烷基、(crC8)雜環烷基、芳基及雜芳基,其各 自係選擇性地經以一或多個齒原子或側氧基取代; 及 R·2為線性或分支(CrC8)院基及 其醫藥上可接受之鹽。 式(IE)化合物之實例包括: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-一氣-6b-(2-經基-乙酿基)-5-經基-4a,6a-二曱基 -4丑,41),5,6,61613,8,9,9\10,1(^,1013,11,12-十四氫-7-«等-8-吖-戊搭烯并[2,l_a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-6b-(2-經基-乙醯基)_4a,6a-二甲基-8-(1-丙基-丁 基)-4&,413,5,6,6&,61),8,9,9&,10,10&,1013,11,12-十四氫-7_〇等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5_ 羥基-4a,6a-二甲基-8-(3-曱基-丁基)-2-側氧基 -2,4&,41),5,6加,8,9,9&,10,1(^,101),11,12-十四氫-7』等-8-。丫-戊 101108588 20 201247697 搭細弁[2, l-a]非-6b-硫代魏酸S-氣甲基自旨; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 經基-6b-(2-經基-乙酿基)-4a,6a-二甲基-8-(3-甲基-丁 基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»号-8-σ丫-戍搭稀并[2,l-a]菲-2-@同; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基-8-(1-丙基-丁 基)-2,4\413,5,6,63,8,9,93,10,1〇3,101),11,12-十四氫-7-4_8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(1-丙基-丁 基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-«号-8· 吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(3-曱基-丁 基)_4&,41),5,6,61613,8,9,9\10,108,101),11,12_十四氫-7-<^-8-α丫-戍搭稀弁[2,l-a]非-2-嗣, (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-甲基-丙基)-4b, 12·二氟-5-羥基-6b-((S)-2-羥基·乙醯基)-4a,6a-二 甲基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫·7-α号-8-σ丫-戊搭細并[2,l-a]非-2-酉同, (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 101108588 21 201247697 羥基-4a,6a-二曱基-8-(3-曱基-丁基)-2-側氧基 -2,4&,41),5,6,618,9,93,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(1-丙基-丁 基)-2,4&,415,5,6,618,9,93,10,10\1013,11,12-十四氫-7-崎-8-吖 -戊搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,618,9,9&,10,1〇1101),11,12-十四氫-7-»等-8-吖_戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-曱 基-丙基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫_7_ 崎 _8_吖戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5_ 羥基-4a,6a-二甲基-8-(3-曱基-丁基)-2-側氧基 -2,4&,仆,5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(卜丙基-丁 基)-2,43,仆,5,6,68,8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8-吖 101108588 22 201247697 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二氣-5-輕基-4a,6a-二曱基-2-侧氧基 -2,4&,41),5,6,6&,8,9,93,10,10&,101),11,12-十四氫-7-'^-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-((S)-l-乙基-2-甲 基-丙基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7,#-8-吖-戊 搭稀弁[2,1-a]非-6b-硫代叛酸S-說甲基酉旨。 依據本案所述類似程序及方法可獲得下列式(IE)本發明 化合物: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-曱 基-丙基)-4b,12-二氧-5-輕基-4a,6a-二曱基-2-側氧基 -2,4&,仆,5,6,6\8,9,9&,10,10&,101),11,12_十四氫-7_哼-8-吖-戊 搭稀并[2,1-a]菲-6b-硫代叛酸S-氣曱基自旨。 於一較佳具體例中,本發明係有關於通式(IF)化合物
101108588 23 201247697 其中
Ri為·(CHdn-Z-fCHdn’-Rjj,其中η為 1 及η’為ο ; -Ζ為單鍵; -R3為氟原子; R2係選自於由下列所組成之組群: -線性或分支(CrC8)烧基、(Cl-C6)烧氧基、(c「c6)齒烷基, 選擇性地經以一或多個CN基取代; --(CH2)mR6,其中Rs係選自於由下列所組成之組群: (CH:8)環烷基、(c^C8)雜環烷基、芳基、芳基氧基、芳基 硫基、及雜芳基,其各自係選擇性地經以選自於由下列所 組成之組群巾之-或多個取代基取代:職基、〇Η、函原 子、CN、ΝΗ2、Ν02、線性或分支(Ci_Q成基、(Ci_C6)烧氧 基芳基、(crc6)經基烧氧基、(Ci_C6)齒烧氧基、直鍵或 分支(CVC6);J^氧基甲醯基、(Ci_C6)絲祕、芳硫基、及 (Ci-C6)烷基磺烷基,其中mg〇或丨至3之整數; 但限制條件為R2非為4·氣-苄基; 及其醫藥上可接受之鹽。 更明確s之,本發明係有關於通式(IG)化合物 101108588 24 201247697
其中 R^-(CH2)n-Z;-(CH2)n’-R3,其中n為 ,為〇 ; -Ζ為單鍵; -Κ·3為氟原子; R·2係選自於由下列所組成之組群: -線性或分支(crc8)烷基; -_(CH2)mR6,其中Re係選自於由(c^C8)環烷基、芳基及雜 芳基所組成之組群,其各自係選擇性地經以選自於由鹵原 子、線性或分支(Q-Q)烧基、(CrC6)燒氧基、(CrC6)烧氧 基曱醯基及(CrC6)烧基硫烧基所組成之組群中之一或多個 取代基所取代,其中m為0或1至3之整數; 但限制條件為R2非為4-氯-苄基; 及其醫藥上可接受之鹽。 於一較佳具體例中,於式(IG)化合物中,烷基 或_(CH2)mR6,此處m為1及R6為選擇性地經取代之雜芳基。 以實例中所述類似程序獲得之其它式(IG)化合物為下列: 101108588 25 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-經基-乙酿基)-5-經基-4a,6a-二曱基-8-(4-甲基-节 基)-43,41?,5,6,6&,613,8,9,9110,1〇3,1013,11,12-十四氫,7-«号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二氟-6b-(2-羥基-乙醯基)-5-羥基-4a,6a-二曱基 -4\41),5,6,6161),8,9,9&,10,1〇1101),11,12-十四氫-7“等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-羥基-乙醯基)-5-羥基-4a,6a-二甲基-8-苯基 -4&,41),5,6,6\61),8,9,9\10,1(^,1013,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-.一氣-6b-(2-經基-乙酿基)-5·經基-4a,6a- —曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-哼-8-吖-戊搭烯并[2,l-a]菲-2-_。 於一較佳具體例中,本發明係有關於通式(IH)化合物 101108588 26 201247697
其中
Ri為(CHJnKCHJn’-Ra,其中n為〇及n,w ; -Z為-S-; -R3為氟原子; R2係選自於由下列所組成之組群: -線性或分支(CrC8)燒基、(Crc6)烧氧基、(C烧基, 選擇性地經以—或多個CN基或㈣子取代; _(cH2)mR6,其中&係選自於由下列所組成之組群· (eve:8)環烧基、((^8)雜環燒基、芳基、芳基氧基、芳基 硫基、及雜芳基,其各自係選擇性地經以選自於由下列所 、、且成之組群中之-或多個取代基取代:侧氧基、、齒原 子N NH2、NO〗、線性或分支(Ci_C6)院基、線性或分支 (CrC6)_烷基、線性或分支(CrC6)烷氧基、芳基、(crC6) 經基烧氧基、(Cl_C6)自炫氧基、(CVC6)烧氧基甲醯基、(Q-Q) 烧基叛基、芳硫基、及(CrC6)烧基績烧基,丨中^❹幻 至3之整數; 101108588 27 201247697 但限制條件為R既非為 疋非為4_氣-苄基也非為丙基笨; 及其醫藥上可接受之鹽。 更月確。之,本發明係有關於通式叫化合物
(IL) 其中 ’其中η為0及η’為1 ; R^-(CH2)n-Z-(CH2)n,-r3 -Z 為-S, -R3為氟原子; R2係選自於由下列所組成之組群: (CVC8) -選擇性地經H或乡個自原子取代之線性或分支 烷基; • -(CH2)mR6,其中r6係選自於由(C3 C8)環烧基、芳基、芳 氧基、方硫基及雜芳基所組成之組群,其各自選擇性地經 以選自於㈣原子、線性或分支(CrC6成基、線性或分支 (CrC6)_烷基、線性或分支(Ci_Q)烧氧基、(c烧氧基 甲醯基、及(CrC6)烷基硫烷基所組成之組群中之一或多個 取代基取代,其中m為〇或1至3之整數; 101108588 28 201247697 但限制條件為Rz既非為4_氯-节基也非為丙基_苯; 及其醫藥上可接受之鹽。 於一較佳具體例中,於式(IL)化合物中,, m為1及R6為選擇性地經取代之芳基或雜芳基。 以實例中所述類似程序獲得之其它化合物為下列: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基-8-(5-甲基-噻吩-2-基甲 基)_2,4&,41),5,6,6\8,9,9110,10\101),11,12-十四氫-7-»等-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5_ 經基-8_(4-甲氧基_卞基)_4a,6a·二曱基-2-側氧基 -2,4&,朴,5,6,6屯8,9,9&,10,103,1013,11,12-十四氫-7“号-8-。丫-戊 搭烯并[2,l-a]菲_6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基_4a,6a-二曱基-8-(3-曱基-丁基)-2-側氧基 -2,4&,41),5,6,6&,8,9加,10,1(^,1013,11,12-十四氫-7“号-8_。丫_戊 搭稀并[2,l-a]雜-6b-硫代叛酸S·氟曱基酉旨, (4&8,仆11,53,如8,6511,9&8,1(^8,1(^8,128)-8-環戊基曱基 -4b, 12-二氣·5-起基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,63,8,9,9&,10,1(^,101),11,12-十四氫-7-崎各〇丫-戊 搭烯并[2,1-a]菲-6b-硫代叛酸S-氣曱基醋; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5_ 101108588 29 201247697 羥基-4a,6a-二曱基-2-側氧基-8-(4-丙基-苄 基)-2,4&,41?,5,6,63,8,9,93,10,1〇11013,11,12-十四氫-7,哼-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5_ 羥基 -4a,6a-二曱基-8-(3-曱基-苄基)-2-側氧基 -2,43,仆,5,6,6\8,9,9&,10,10\101),11,12-十四氫-7“号-8-吖,戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-((S)-氟曱基)醋; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基·8-(5-氣-噻吩-2-基-曱 基)-2,4&,41),5,6,6&,8,9,9&,10,103,101),11,12-十四氫_7-»等_8-吖 -戊搭烯并[2,1-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-8-(4-甲基-苄基)-2-側氧基 -2,4&,41),5,6,618,9,9&,10,1(^,1013,11,12-十四氫-7^号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4日8,仆11,58,6&3,6511,9&8,1〇38,1(^8,128)-8_(4-第三-丁基-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41?,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟·5-羥基-4a,6a-二曱基-2-侧氧基-8-(2-苯基硫烷基-乙 基)-2,4&,41),5,6,6&,8,9,9&,10,1〇3,1015,11,12-十四氫-7-«等-8-吖 10110858S 30 201247697 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 經基-4a,6a-二甲基-2-側氧基-8-(1-丙基-丁 基)-2,4&,413,5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖 -戊搭烯并[2,1-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基-8-(2-苯氧基-乙 基)-2,4\413,5,6,6&,8,9,9110,10\101),11,12-十四氫-7-°号-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-弘 經基_4a,6a-二甲基-2-側氧基-8-(5-氣-α夫喃-2-基-曱 基)-2,4&,仆,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-°号-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b, 12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,618,9,9&,10,1(^,1013,11,12-十四氫,7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(5-曱基·噻吩-2-基曱 基)-2,4&,41),5,6,6&,8,9,93,10,10&,101),11,12-十四氫-7-«等-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 101108588 31 201247697 羥基-8-(4-曱氧基-苄基)-4a,6a-二曱基-2-侧氧基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,105,11,12-十四氫-7-'»号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-8-(3-曱基-丁基)-2-側氧基 •2,4141),5,6,6还,8,9,9&,10,10&,101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4&8,仆11,58,6&3,6匕艮9&8,10&8,1(^3,128)-8-環戊基甲基 -4b, 12-二氟-5-經基-4a,6a-二甲基-2-侧氧基 -2,4\仆,5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-哼-8-吖-戊 搭烯并[2,1-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(4_丙基-苄 基)-2,4\415,5,6,6&,8,9,93,10,10&,1013,11,12-十四氫-7-哼-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)_4b,12-二氟-5·羥基 -4a,6a-二曱基-8-(3-曱基-苄基)-2-側氧基 -2,43,41),5,6,63,8,9,9&,10,10&,1013,11,12-十四氫,7-»等-8-吖-戊 搭烯并[2,1 -a]菲-6b-硫代羧酸S-((S)-氟曱基)酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基-8-(5-氯-噻吩-2-基-曱 基)-2,4&,仆,5,6,如,8,9,9&,10,1(^,1013,11,12-十四氫-7-崎-8-吖 101108588 32 201247697 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-8-(4-甲基-苄基)-2-側氧基 •2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+®lL-7-4-8-%j 搭稀并[2,1-a]菲-6b-硫代缓酸S-默曱基酉旨; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4JS-T*-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+®&-7-#-8-Wj 搭稀弁[2,1-a]菲-6b-硫代緩酸S-氟甲基醋; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基-8-(2-苯基硫烷基-乙 基)-2,4&,41),5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-»等-8-口丫 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(1·丙基-丁 基)_2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+izg|L-7-4-8-V -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(2-苯氧基-乙 基)-2,4\41),5,6,63,8,9,9&,10,103,1013,11,12-十四氫-7-»号-8-口丫 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5- 101108588 33 201247697 經基_4a,6a-二曱基-2-侧氧基-8-(5-氣-咬喃-2-基-曱 基)-2,4\413,5,6,618,9,93,10,103,101),11,12-十四氫-7-»等-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12-二氣-5-經基-4a,6a-二曱基-2-側氣基 -2,4&,41?,5,6,618,9,9&,10,1(^,101),11,12-十四氫-7_»号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基•丁 基)_4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4&,41),5,6,6\8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-丁氧 基_ ~基)_4b,12-二敗-5-經基_4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7-4-8-。丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-丁氧基-苄 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+ra&-7-#,8-V4 搭稀并[2,1-a]菲-6b-硫代缓酸S-敗曱基酉旨; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-8-(5-曱基-呋喃-2-基曱基)-2-側氧基 -2,4\41),5,6,63,8,9,9&,10,10&,101),11,12-十四氫,7-»等-8-吖-戊 101108588 34 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基-(5-甲基硫烷基-噻吩-2-基曱 基)-2,414\5,6,6\8,9,9&,10,10&,1013,11,12-十四氫-7-»号-8-吖 •戊搭烯并[2,l-a]菲-61>硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-((S)-l-乙基-2-曱 基-丙基)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基 -2,4\41>,5,6,6&,8,9,9110,1(^,101>,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基_2_侧氧基-8-(3,3,3-三氟-丙 基)-2,4\41),5,6,6&,8,9,93,10,1(^,1013,11,12-十四氫-7-谔-8_吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆艮58,6&8,6511,938,1〇38,1(^5,128)-8-環丙基甲基 -4b,12-二氣-5-經基-4a,6a-二曱基-2-側乳基 2,4&,41?,5,6,6&,8,9,9&,10,1〇3,1015,11,12-十四氫-7-"等,8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2dSCS-6 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 •2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12_ 十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆尺,58,6&8,6乜艮9&8,1(^3,1(^8,128)-8-二環[2.2.1]庚 101108588 35 201247697 -2-基-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41?,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7_«等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基 -4a,6a-二甲基-8-((S)-l-曱基-1H-吲哚-3-基-曱基)-2-側氧基 -2,4&,41),5,6,6&,8,9,93,10,103,1013,11,12-十四氫-7-〇号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基-8-間-曱苯基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫_7-»号_8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸8_氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-鄰-曱苯基 -2,4&,41),5,6,63,8,9,9&,10,1(^,101),11,12-十四氫-7-«号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-對-曱苯基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-»号-8-吖-戊 搭烯并[2,l-a]菲-6卜硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_8-(3-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4日,41),5,6,63,8,9,9&,10,1(^,1013,11,12-十四氫-7,》号-8-吖-戊 101108588 36 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4汪5,仆11,58,6511,9&8,1(^8,1(^8,128)-413,12-二氟_8-(4_氣 本基)-5-經基-4a,6a-二曱基-2-側氧& 2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12--hug4-7-x»n〇Yj 搭烯并[2,1 -a]菲-6b-硫代羧酸S-((S)-氟甲基)酯; (4&3,仆11,58,6&8,6匕11,9&3,1(^3,1(^8,128)-41),12_二氣5 輕基-4a,6a·二曱基-2-側氧基-8- 〇比咬_3基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+E3|^7-〇nDYj 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-:i_8-(3j 本基)-5-沒基-4a,6a-二曱基-2-側氧其^ ,2如,413,5,6,6&,8,9,9&,10,1(^,101),11,12-十四氣_7-〇号_8_。丫_戊 搭烯并[2,1 _a]菲-6b-硫代羧酸S-((S)-氟曱基)輯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12_ 二敦 經基-4a,6a-二甲基-2-側氧基-8-(4-三敗曱基_笨 基)-2,4汪,41),5,6,63,8,9,9&,10,10&,101),11,12-十四氫-7-»号-8-〇丫 •戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯。 依據本案所述類似程序及方法,獲得下列化合物: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-曱 基-丙基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-。号-8-吖-戊 搭烯并[2,l-a]菲_6b-硫代羧酸S-氟曱基酯; 101108588 37 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基-8-丙基 -2,43,仆,5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7“等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基-8-吡啶-3-基 -2,4141),5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基-8- β塞。坐-4-基 -2,4&,41),5,6,如,8,9,9已,10,10&,101},11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-8- 唑-2-基-2-側氧基 -2,4&,41),5,6,如,8,9,93,10,10&,101),11,12-十四氫-7-哼-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2·側氧基-8-噻唑-2-基曱基 -2,43,41),5,6,6\8,9,9&,10,1〇11013,11,12-十四氫-7-4-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-8-(2-咪唑-1-基-乙基)-4a,6a-二曱基-2-側氧基 101108588 38 201247697 -2,4&,41),5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4已8,仆11,58,638,6匕11,9&8,10&8,1(^8,128)-8-(2-環己基-乙 基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,63,8,9,9&,10,10&,1013,11,12-十四氫-7-。等-8_吖-戊 搭烯并[2,1-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二曱基-2-侧氧基-8-(3- α比咬-3-基-丙 基)-2,4\41),5,6,618,9,9&,10,10&,1013,11,12-十四氫-7-»等-8_吖 -戊搭烯并[2,1-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12·二氟-8-咬喃-3-基-5-經基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-+ © 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS510aS,10bS,12S)-4b,12·二氟-5-羥基-8-(lH-吲哚-3-基甲基)-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-Ί- ® 搭烯并[2,l-a]菲-6b_硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基_8-喹啉-7-基甲基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-+ va -8-°Υ-^ 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; 101108588 39 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并噻唑-2-基曱基-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41>,5,6,618,9,9&,10,10&,101),11,12-十四氫-7-»等-8,吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆11,53,如8,6511,9&3,10&3,1(^3,128)-8-二環[2.2.1]庚 -2-基-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基 -2,43,41?,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-«1等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-啥琳-5-基曱基 -2,4141),5,6,63,8,9,9&,10,10&,101),11,12-十四氫-7-崎-8-吖-戊 搭稀并[2,1-a]菲-6b-硫代缓酸S-氣曱基S旨, (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基-8-喹啉-2-基曱基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+E9lL,7-4-8,j 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并呋喃-3-基-4b, 12-二氟-5-羥基-4a,6a·二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,1〇3,1013,11,12-十四氫-7』号_8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并[1,3]二 呃-5-基-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 101108588 40 201247697 -2,4及,41),5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-17等-8-〇丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-8-(1-甲基-1H-吲哚-2-基)-2-側氧基 -2,4\41),5,6,6\8,9,9110,1(^,1013,11,12-十四氫_7-«等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基-8-(1-曱基-1H-吲哚-3-基曱 基)-2,4心41),5,6,63,8,9,93,10,10&,1013,11,12-十四氫-7-»号-8,吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-(1-曱基-1H-咪唑-4-基曱 基)_2,4&,413,5,6,6&,8,9,93,10,10\101),11,12-十四氫-7-崎-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_4b,12-二氟-5-輕基-8-(1Η·D弓卜朵-2-基曱基)-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,6&,8,9,9110,1(^,101},11,12-十四氫-7-口等,8-。丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,63,8,9,9\10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯.; 101108588 41 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12_ 二氟-5-經基-4a,6a-二曱基-2-側氧基-8-對-曱本基 -2,4\413,5,6,618,9,9110,1〇11015,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-8-(4-曱氧基-苯基)-4a,6a-二曱基-2-側氧基 -2,4\41?,5,6,618,9,9110,1〇11013,11,12-十四氫-7-<»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5_ 羥基-4a,6a-二曱基-2-側氧基-8-鄰-曱苯基 -2,43,朴,5,6,6心8,9,93,10,1〇1101),11,12-十四氫-7-«等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣-苯 基)-4b,12·二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,43,45,5,6,618,9,9&,10,10&,101),11,12-十四氫-7-<^-8-吖_戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-間-曱苯基 -2,4&,41),5,6,618,9,9&,10,1〇1101),11,12_十四氫,7-»号_8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-8-(3·甲氧基-苯基)-4a,6a-二曱基-2-側氧基 101108588 42 201247697 -2,4\41),5,6,6&,8,9,9&,10,10\101),11,12-十四氫-7-哼-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯。 以實例中所述類似程序獲得之其它化合物為下列: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(1-丙基-丁 基)-4&,仆,5,6,6&,613,8,9,9&,10,10\101),11,12-十四氫-7-哼-8-吖·戊搭烯并[2,l-a]菲-2-酮; (4巳5,仆11,58,6&8,65艮9&8,1(^8,1(^8,128)-8-(4-第三-丁基-苄基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -41413,5,6,6&,615,8,9,9&,10,10&,101),11,12-十四氫-7-«号-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(4-丙基-苄 基)-4&,41?,5,6,6&,61),8,9,9牡,10,10&,101),11,12-十四氫,7-'»等,8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12-二氣-5-經基-6b-(2-經基-乙酿基)-4a,6a- —曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-o号-8-o丫_ 戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(3-曱基-丁 基)_4&,41),5,6,6&,61),8,9,9&,10,10&,1013,11,12-十四氫-7-'1等-8- 101108588 43 201247697 吖-戊搭烯并P,l-a]菲-2-酮》 於較佳具體例中,本發明係有關於通式(IM)化合物
RA,(CH2)n-Z-(CH2)n,-R3,其中η為0及η,為 1 ; Ζ為單鍵; 其中 R3 為-ΟΗ ; R2係選自於由下列所組成之組群: -線性或分支(Ci_C8)烷基; —(C^WinR6’其中I係選自於由(C3_C8)環烷基所組成之組 群,其中m為〇或1至3之整數及 其醫藥上可接受之鹽。 具體例中’本發明係有關於通式_匕合物 101108588 201247697
其中 RA_(CH2)n-Z-(CH2)n’-R3,其中 n為〇&n,為工; Z為單鍵; R3 為-OH ; R2為-(CH2)mR6 ’其中Re為芳基其係選擇性地經以選自於 由下列所組成之組群中之一或多個取代基取代:_原子、 CN、C〇NH2、NHC(〇)H、線性或分支(CrC6)烷基 c ' ^6) 烷基磺醯基、線性或分支(CrC6)鹵烷基、線性或分支(CVC6) 鹵烷氧基、(CrC6)烷氧基甲醯基、(CrC6)烷氧基磺醯基、 (CrC6)_烷基績醯氧基、(crC8)環烧基、(CrC6)雜環烷武 胺基磺醯基、及雜芳基,及m為0及其醫藥上可接受之_。 以實例中所述類似程序獲得之其它化合物為下列: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,l2-二氣 5 羥基-6b-(2-羥基-乙醯基)-4a,6a·二曱基-8-(1-丙基丁 S)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+Eg^_7_n^8 吖-戊搭烯并[2,l-a]菲-2-酮; 101108588 45 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12-二 It -5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7“等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(3-曱基-丁 基)-4&,41),5,6,61613,8,9,9110,1〇3,101),11,12_十四氫-7-«等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基_6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-對-曱苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-α等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5_ 羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-間-曱苯基 4\413,5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7-噚-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-:l-8_(4-‘-苯基)-5-羥基-6b-((S)-2-羥基-乙醯基)-4a,6a-二曱基 -4丑,仆,5,6,6&,615,8,9,9&,10,1(^,1013,11,12-十四氫-7_哼-8-吖· 戍搭稀弁[2,1-a]菲-2-嗣; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基 101108588 46 201247697 •4\41),5,6,6&,61),8,9,93,10,1(^,101),11,12-十四氫,7-噚-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(4-三氟曱基-苯 基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-碍-8-吖-戊搭婦并[2,l-a]菲-2-酮; (4&3,仆11,53,6511,9&8,1(^8,1(^8,128)-41),12-二氟-8-(3-氟-苯基)-5-羥基-6b-((S)-2-羥基-乙醯基)-4a,6a-二曱基 -4\413,5,6,61613,8,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-鄰-曱苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-(4-氣-3-曱基-苯 基)-4b,12 -二氣-5-輕基-6b-((S)-2 -經基-乙酿基)-4a,6a-二曱 基-4\41),5,6,6&,613,8,9,9&,10,1(^,101),11,12-十四氫-7-4-8-吖 -戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-3-三氟 甲基-苯基)-4b,12-二說-5-經基-6b-(2-經基-乙酿基)-4a,6a-二 曱基-4\41),5,6,6汪,613,8,9,9110,1(^,101),11,12-十四氫,7-口号-8-吖-戊搭烯并[2,l-a]菲-2_酮; 101108588 47 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,4-二氯-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4\41),5,6,6161),8,9,9&,10,10&,101),11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,l〇bS,12S)-8-(4-溴-笨 基)-4b,12-二氣1 -5-經基-6b-(2-經基·乙酿基)-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12_ 十四氫-7-0 等-8- 口丫-戊搭烯并[2,l-a]菲-2-酮; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS)-4b-氟-5-羥基 -6b-(2-羥基-乙醢基)-4a,6a-二甲基-2-側氧基 -2,4&,41),5,6,63,613,9,9&,10,10&,101),11,12-十四氫-7-°号-8-〇丫- 戊搭烯并[2,l-a]菲-8-基]-苯曱腈; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 •5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,61615,9,9&,10,10\1013,11,12-十四氫-7-崎-8-吖-戊搭烯并P,l-a]菲-8-基]-苯曱醯胺; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-(4-二乱曱氧基-苯 基)_4&,41?,5,6,6&,61),8,9,9&,10,103,1013,11,12-十四氫-7“等_8-α丫-戊搭婦并[2,1-a]菲-2-酉同; 曱烷磺酸4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b, 12-二氣-5-經基_6b-(2-經基-乙酿基)-4a,6a-二曱基-2-側氧基 101108588 48 201247697 -2,48,41),5,6,6&,613,9,9&,10,10&,1013,11,12-十四氫-7-<1等_8-口丫-戊搭烯并[2,l-a]菲-8-基]-苯基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-環己基-苯 基)-4b,12-二氣-5-經基-6b-(2-輕基-乙酿基)-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»等-8-吖· 戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(4-噻吩-2-基苯 基)-4玨,415,5,6,6&,61),8,9,9&,10,1〇3,101),11,12-十四氫-7-"等-8-吖-戊搭烯并[2,l-a]菲-2-酮; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,6&,61),9,9\10,10&,101),11,12-十四氫-7-«等-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯曱酸曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-8-(4-曱烷磺醯基-苯基)-4a,6a-二 曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»号-8-吖-戊搭烯并[2,l-a]菲·2-酮; 3-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2·羥基·乙醯基)-4a,6a-二曱基-2-側氧基 -2,4\415,5,6,63,615,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯曱腈; 101108588 49 201247697 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基·乙酿基)-4a,6a-二甲基-2-側氧基 -2,43,41?,5,6,6&,613,9,93,10,103,1015,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯磺醯胺; (4汪3,仆11,53,6&8,6511,938,10&8,1(^3,128)-8-(4-環丙基-苯 基)_4b,12 -二氣-5·經基-6b-(2-經基-乙酿基)-4a,6a-二甲基 -4\41>,5,6,6161),8,9,9&,10,1(^,1013,11,12-十四氫-7-崎,8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,58,如8,6511,9&8,1(^8,1(^8,128)-8-(4-第三-丁基-苯基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 •4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-» 号-8-吖-戊搭烯并|;2,l-a]菲-2-酮; N-{4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 鼠-5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,6\613,9,9&,10,1(^,101),11,12-十四氫-7-噚-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯基卜甲醯胺; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(3-三氟曱基-苯 基)-4&,41),5,6,6161),8,9,9&,10,103,1013,11,12-十四氫-7-4-8· 吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(3-三氟曱氧基-苯 101108588 50 201247697 基)-4\41),5,6,63,61),8,9,9&,10,1〇3,101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3/^-,*)-4b,12-二氣-5-沒基-6b-(2-經基-乙酿基)-4a,6a- —曱基 -4&,仆,5,6,6&,61?,8,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并噻唑-6_ 基-4b, 12-二氣-5-經基-6b-(2-經基-乙酿基)-4a,6a- —曱基 ,4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-« 号-8-吖· 戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-8-(4-羥基-苯基三氟甲烷磺酸 根)-4a,6a-二甲基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12- + 四氫-7-哼-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆尺,58,6&8,6511,9&8,1(^8,1(^8,128)-8-(3-環丙基-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4&,41>,5,6,6161),8,9,9&,10,1(^,101),11,12-十四氫-7-"号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S>4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a_二曱基-8·(4_哌啶-4-基甲基_ 苯基)-4&,415,5,6,6161),8,9,9&510,10&,1013,11,12,十四氫-7-口等 -8-吖-戊搭烯并[2,l-a]菲-2-酮。 101108588 51 201247697 於一較佳具體例中,本發明係有關於通式(IN,)化合物
(IN’) 其中 RA-(CH2)n-Z-(CH2)n,-R3,其中!!為0及以為!; Z為單鍵; R3 為-OH ; R_2為-(CH2)mR6 ’其中&為雜芳基及m為〇及其醫藥上可接 受之鹽。 以實例中所述類似程序獲得之其它化合物為下列: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二敦 _5_ 羥基-6b-(2-羥基-乙醯基>4a,6a-二甲基-8-嗤琳_6_基 -43,413,5,6,6&,61),8,9,93,10,10&,1015,11,12-十四氫_7-4_8-〇丫 戊搭烯并P,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二敦 _5· 羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8·吡咬_3•基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫等·8_口丫 _ 戊搭烯并[2,l-a]菲·2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并嚷 α坐卜 101108588 52 201247697 基-4b,12-二氟-5·羥基-6b-(2-羥基-乙醯基)-4a,6a_二曱基 -4汪,41),5,6,6&,613,8,9,9&,10,10&,1013,11,12-十四氫-7-°等-8-吖-戊搭烯并[2,l-a]菲-2-酮。 須瞭解本發明涵蓋前述特定及較佳組群及具體例之全部 組合。 後文中,式(I)、(I,)、(IA)、(IB)、(1C)、(ID)、(IF)、(IG)、 (IH)、(IL)、(IM)、(IN)化合物及其醫藥上可接受之鹽及溶 劑合物係稱作為「本發明化合物」。 本發明之較佳化合物之實例為: 物 化學名稱 ~~'~'~~ 10 — (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-5^ET^XT 丁基)-41>,12-二氣-5-經墓-61>(2-經基-乙酿基)_436&_^ 曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-~fizg’|i7* «等-8-吖-戍搭烯并丨2,l-al菲-2-酮 w 11 — (4aS,4bR,5 S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-4bJ2r~^T~^--8-(4-氣千基)-5-經基-6b-(2-經基-乙酿基)-4a,6a-二甲某 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫寻 8 吖-戊搭烯并[2,l-al菲-2-酮 · _ 12 (4aS^bR,5S,6aS,6bR,9aS,10aSJ0bSJ2S)-4b,nTEr|^5r 一呈基-6b-(2-i基-乙ίί基)-4a,6a-二曱基-8-"塞吩-2-基甲美 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,li,12-十四氫_7_。等 $ 吖-戊搭烯并丨2,1-al菲-2-酮 ^ vT~~ (4aS,4bR,5S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-4b,ΪΪΓΞΓΙ^Γ 0夫喃_2_墓甲基經墓_6b-(2-經基-乙酿墓)_4a,6a-二曱義 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫_7-。等 $ 。丫-戊搭烯并丨2,l-al菲-2-酮 14 (4aS,4bR,5 S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-8-(2-lTSry~ 基)-4b,12-二氣-5-經基-6b-(2·經基-乙 4基)-4a,6a-二甲 基-4^415,5,6,6木61),8,9,93,10,10&,101),11,12-+四氫_7_〇寻 -8-吖-戊搭烯并丨2,l-al菲-2-酮 101108588 53 201247697 15 3-[(4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-4b,12-二 氣-5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-2-側氧基 _2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,l 1,12·十四氫-7-0 咢-8· 吖-戊搭烯并丨2,l-al菲-8-基甲基1-苯甲酸甲基酯 16 (4&5,物11,58,6&8,6611,938,1(^8,1(^8,128)-8-環己基曱 基-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲 基-4屯41),5,6加,61),8,9,9&,10,1(^,1015,11,12-十四氫-7-口等 -8-吖-戊搭烯并丨2,l-al菲-2-酮 17 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-έΐ>(2-經基-乙酿基)-4a,6a-二曱基-8-(4-曱基硫 烷基-苄基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12- + 四氫-7-»等-8-吖-戊搭烯并f2,l-al菲-2-酮 18 (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-((R,S)-第二 -丁基)-4b,12-二氣-5-經基-6b-(2-經墓-乙酿基)-4a,6a-·一 曱基-4木41),5,6,63,613,8,9,9木10,1(^,1015,11,12-十四氫-7-»等-8-。丫-戊搭烯并「2,l-al菲-2-酮 19 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環戊基甲 基-4b,12-二氣-5-經喜>-6b-(2-經基-乙酿基)-4a,6a-· —曱 基-43,413,5,6,6461),8,9,9410,1(^,1015,11,12-十四氫-7-»等 -8·。丫-戍搭烯并f2,l-al菲-2-酮 20 4- [(4aS,4bR,5 S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-4b, 12-二 氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,6b,9,9a,10,1 Oa,10b,11,12-十四氫-7-碍-8-。丫-戊搭烯并「2,l-al菲-8-基曱基1-笨甲酸第二丁酯___- 21 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-^ 基)_4b,l2-二氣-5-經基-6b-(2-經基-乙酿基)-4a,6a- — ^ 基-4&,牝,5,6,6&,6匕,8,9,9&,10,1(^,101),11,12-十四氫-7-巧 -8-°丫 戍搭▲并『2,l-al 菲-2-明 __.一rr— 23 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 5 •5_羥基-6b-(2_羥基-乙醯基Ha,6a-二甲基-8_(1-丙基·丁 基)-4&,牝,5,6,63,61),8,9,93,10,10木101?,11,12-十四氫-7-谔-8-吖-戊搭烯并丨2,l-al菲-2-酮 24 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-厂 基-苄基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6|_ 二甲基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+®l -7-崎-8-吖-戊搭烯并丨2,l-al菲-2-酮 _一 25 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 g -5-羥基-6b-(2-羥基-乙酿基)-4a,6a-二甲基-8-(4-丙基1 基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫 _7-崎-8-吖-戊搭烯并丨2,1-al菲·2-酮 -- 101108588 54 201247697 26 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12-二象j-5-經基-6b-(2-經墓-乙酿基)-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-^-8-吖-戊搭烯并丨2,l-al菲-2-酮 27 (438,^11,58,638,651^938,1(^8,1(^8,128)-415,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(3-曱基-丁 基)-4\牝,5,6加,613,8,9,9屯10,1(^,101),11,12-十四氫-7-。咢-8-吖-戊搭烯并「2,l-al菲-2-酮 28 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(5-甲基硫 烷基-噻吩-2-基曱基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b, 11,12-十四氫-7-»号-8-吖-戊搭烯并丨2,l-al菲-2-酮 29 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-甲基 -丙基)-4b,12-二氣-5·經基-6b-((S)-2-經基-乙酿 基)-4a,6a-二曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll, 12-十四氫-7-°等-8-吖-戊搭烯并「2,1-al菲-2-酮 30 (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS, 1 ObS,12S)-8-(4- 丁氧基-卞基)-4b,12-二氣-5-經基·61)-(2-經墓-乙酿基)-4a,6a-二 甲基-4\牝,5,6,63,613,8,9,9110,1(^,1013,11,12-十四氫-7-崎-8-。丫-戊搭烯并酮 31 (4&8,扑11,58加8,6511,938,1(^8,1(^8,123)-8-(2-環己基-乙基)-4b,12-二氣_5-經基-6b-(2-經汰-乙酿基)-4a,6a-二 甲基-4屯41),5,6,6木61),8,9,93,10,1〇8,101),11,12-十四氫-7-«等-8-吖-戊搭烯并丨2,l-al菲-2-酮 32 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-6b-((S)-2-羥基-乙醯基)-4a,6a-二甲基-8-(1-甲基-1H-吲哚-3-基曱基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a, 10b,ll,12-十四氫-7-谔-8-吖-戊搭烯并丨2,1-al菲-2-酮 33 (4&8,扑11,58,638,65民938,10&8,1058,125)-8-二環[2.2.1] 庚-2-基-4b,12-二敗-5-經基-6b-(2-經基-乙酿基)-4a,6a-二甲基-4&,41>,5,6,63,613,8,9,98,10,1(^,1013,11,12-十四氫 _7-»等-8-吖-戊搭烯并「2,1 -al菲-2-酮 34 (4aS,4bR}5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-(3-0比咬-3-基-丙基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,11,12-十四 氫-7-«等-8-吖-戊搭烯并丨2,l-al菲-2-酮 35 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基-乙酿基)-4a,6a-二甲基-8-(3,3,3-二 氟-丙基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+ra 氪-7-噚-8-。丫-戊搭烯并丨2,l-al菲-2-酮 36 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-8-(2-咪唑-1-基-乙 基)-4a,6a-二曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll, 12·十四氫-7-嘮-8-«丫-戊搭烯并「2,l-al菲-2-酮 101108588 55 201247697 37 (4aS,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b-(R)-氟-12-氟 -5_經基-6b-(2-經基-乙酿基>)-4a,6a-二曱基-δ-啥琳·5-基 曱基-43,牝,5,6,63,沾,8,9,93,10,10\101?,11,12-十四氫-7-«等-8-吖-戊搭烯并「2,l-al菲-2-酮 38 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基乙酿基)-4a,6a-二曱基塞0坐-2-基> 曱基-4a,牝,5,6,6\61),8,9,9〜10,1(^,101),11,12-十四氫-7-。等-8-吖-戊搭烯并「2,1-al菲-2-酮 39 曱烷磺酸 2-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S) -8-(4-氣-节基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧 基-2,4&,413,5,6,63,8,9,9&,10,1(^,1013,11,12-十四氫-7-口等 -8-吖-戊搭烯并丨2,l-al菲-6b-基1-2-側氧基-乙基酯 40 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-乙醯基 -8-(4-氣-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,11,12-十四氫-7-» 咢-8-吖-戊搭烯并『2,l-al菲·2-酮 41 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苄 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4\413,5,6,63,8,9,9&,10,1(^,101),11,12-十四氫-7-哼-8-吖-戍搭烯并丨2,1-al菲-6b-叛酸 42 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-二曱 基-丁基)-4b,12-二氣-5-經基-4a,6a-二甲基-2-側氧; 2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-» 咢-8_ 吖-戊搭烯并『2,l-al菲-6b-羧酸 43 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-氣- > 基)-5-經墓-4a,6a-二曱基-2-側氧; -2,4\41),5,6,63,8,9,9屯10,1〇3,101),11,12-十四氫-7-崎-8-吖-戍搭嫦并丨2,1-al菲-6b-羧酸 44 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二曱基-2-側氧基-8-隹吩_2-基曱墓 -2,4\415,5,6,63,8,9,9木10,1(^,1015,11,12-十四氫-7-崎-8-。丫-戊搭烯并丨2,1-al菲-6b-羧酸 45 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-β夫喃-2-基曱基-5-經基-4a,6a-二曱基-2-側氧基 -2,4a,4b55,6s6a,8,9,9a,10510a,10b,ll,12-+ izg 。丫-戊搭烯并[2,l-al菲-6b-羧酸 46 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二曱基-8-(5-曱基-噻吩-2-基甲基)-2-側 氧基-2,4\41?,5,6,6\8,9,93,10,103,101),11,12-十四氫-7-崎-8-吖-戊搭烯并『2,l-al菲-6b-羧酸 101108588 56 201247697 47 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5_輕基-8-(4_甲氧墓-节基)-4a,6a-二曱基_2·側氧; -2,4a,牝,5,6,6&,8,9,9\10,1〇3,1015,11,12-十四氫-7-崎-8-吖-戊搭烯并「2,1-al菲-6b-羧酸 48 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二甲基-8-(3-曱基-丁基)-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7“等-8-吖-戊搭烯并「2,Ι-a〗菲-6b-羧酸 49 (4&8,物11,53,6&8,仍11,933,1(^3,1(^8,123)-8-環戊基曱 基-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4\413,5,6,6\8,9,9屯10,10&,1015,11,12-十四氫-7-。等-8-吖-戊搭烯并[2,l-al菲-6b-羧酸 50 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-(4-丙基-节 基)-2,4\413,5,6,6&,8,9,9\10,1〇3,101),11,12-十四氫-7-。号 -8-吖-戊搭烯并「2,l-al菲-6b-羧酸 51 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二甲基-8-(3-曱基-苄基)-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-崎-8-。丫-戊搭烯并『2,1-al菲-6b-羧酸 52 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(5-氣-噻吩 -2-基甲基)-北,12-二氟_5-羥基-43加-二甲基-2-側氧基 -2,4\41),5,6,63,8,9,9&,10,1〇3,1015,11,12-十四氫-7-哼-8-吖-戊搭烯并丨2,l-al菲-6b-羧酸 53 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二曱基-8-(4-甲基-节基)-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-口等-8-吖-戊搭烯并『2,1-al菲-6b-羧酸 54 (4aS,4bR,5S,6aS,6bR,9aS, 1 OaS, 1 ObS,12S)-8-(4-第三-丁 基-苄基)-4b, 12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4木41*,5,6,63,8,9,93,10,1〇3,101),11,12-十四氫-7-崎-8-β丫-戊搭烯并f2,l-al菲-6b-羧酸 55 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基 -2-側氧基-8-(2-苯基硫烧基-乙 基)-2,4&,41),5,6,6木8,9,93,10,1(^,101),11,12-十四氫-7-哼 -8-。丫-戊搭烯并[2,1-al菲-6b-羧酸 56 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a·二甲基-2-側氧基-8-(1-丙基-丁 基)-2,43,牝,5,6加,8,9,93,10,1(^,1013,11,12-十四氫-7-口号 -8-。丫 ·戊搭烯并[2,l-al菲-6b-羧酸 57 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-(2-苯氧基-乙 基)-2,4&,牝,5,6,6已,8,9,9&,10,1〇3,101),11,12-十四氫-7-口号 -8-。丫-戊搭烯并「2,l-al菲-6b-羧酸 101108588 57 201247697 58 (4aS,4bR,5 S,6aS,6bR,9aS, 1 OaS,1 ObS, 12S)-8-(5-氣-呋喃 -2-基曱墓)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-崎-8-吖-戊搭烯并「2,l-al菲-6b-羧酸 59 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氩-7-崎-8-吖-戍搭烯并「2,l-al菲-6b-缓酸 60 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4士415,5,6,63,8,9,93,10,1(^,1013,11,12-十四氩-7-谔-8-0丫-戊搭烯并丨2,l-al菲-6b-叛酸 61 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-丁 氧基-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-» 等-8-吖-戊搭烯并「2,l-al菲-6b-羧酸 62 (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-(4- 丁氧基-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-«等-8-吖-戍搭烯并「2,l-al菲-6b-羧酸 63 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二曱甲基夫喃-2-基曱基)-2-側 氧基-2,4\41),5,6,618,9,93,10,10&,101),11,12-十四氫-7-崎-8-吖-戍搭烯并丨2,l-al菲-6b-羧酸 64 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二曱墓-8-(5-曱基硫烧基-〇塞吩-2-基甲 基)-2-側氧基-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十 四氫-7-α等-8·吖-戊搭烯并[2,l-al菲-6b-羧酸 65 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-曱基-丙喜·)-41?,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-。号-8-吖-戍搭烯并『2,l-al菲-6b-駿酸 66 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-(3,3,3-二氣-丙 基)-2,43,牝,5,6,63,8,9,93,10,10\1013,11,12-十四氫-7-口号 -8-吖-戊搭烯并『2,1-al菲-6b-羧酸 67 (4&3,处11,58加3,6511,938,1(^3,1(«^,123)-8-環丙基甲 基-4b,12-二敗-5-經基-4a,6a-二曱基-2-側氧▲ -2,4a,4b55,6,6a,8,9,9a,10,10a,10b,ll,12--h E9 l^-7-af-8-吖-戍搭烯并[2,1-al菲-6b-緩酸 68 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-環己基-乙基)-4b,12-二氣-5-經基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+ 四氫-7“ 等-8-。丫-戊搭烯并f2,l-al菲-6b-羧酸 101108588 58 201247697 69 (4aS,4bR,5S,6aS,6bR,9aS,10aS,1 ObS,12S)-8-二環[2.2.1 ] 庚-2-基-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,63,8,9,93,10,1(^,1015,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,1-al菲-6b-羧酸 70 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二甲基-8-(1-曱基-1H-吲哚-3-基甲基)-2-側氧基-2,4&,牝,5,6,6\8,9,9\10,1(^,1013,11,12-十四氫 -7-崎-8-吖-戊搭烯并『2,l-al菲-6b-羧酸 71 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苄 基)-4b, 12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4\牝,5,6,6&,8,9,93,10,10\101?,11,12-十四氫-7-。号-8-吖-戊搭烯并[2,l-a]菲-6b-硫代羧酸S-(2-側氧基-[1,3]二 β等11東-4-基)醋 72 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苄 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\413,5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-al菲-6b-羧酸甲氧基-甲基-醯胺 73 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二甲基-2-側氧基-8·噻吩-2-基甲基 -2,4\牝,5,6,如,8,9,9&,10,10\101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,1-al菲-6b-緩酸氟甲基酯 74 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-氟-苄基)-5-羥基-4a,6a-二曱基-2-側氧基 -2,4屯413,5,6,63,8,9为,10,1(^,101),11,12-十四氫-7-»等-8-吖-戊搭烯并「2,l-al菲-6b-羧酸氟曱基酯 75 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-乳-节基)-5-經墓-4a,6a-二甲基-2-側氧表 -2,4士41?,5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-«等-8-吖-戍搭烯并『2,l-al菲-6b-缓酸氰基甲基酯 76 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-0塞吩-2-基曱i -2,4屯415,5,6,63,8,9,9\10,10屯1015,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-al菲-6b-羧酸氰基曱基酯 77 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-0夫喃-2-基甲基-5-經基-4a,6a-二甲基-2-側氧基 -2,4木413,5,6,63,8,9,9&,10,1(^,1013,11,12-十四氫-7-崎-8-。丫-戊搭烯并[2,l-al菲-6b-硫代羧酸S-氟甲基酯 101108588 59 201247697 78 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-敦-节基)-5-經基-4a,6a-二甲基·2·側氧基 -2,43,牝,5,6,6\8,9,93,10,10&,101?,11,12-十四氫-7-»号-8-吖-戍搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基酯 79 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-0塞吩-2-基甲基 -2,4\41),5,6,6壮,8,9,93,10,1(^,1013,11,12-十四氫-7-崎-8-。丫-戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基酯 80 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-二曱 基丁基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4\牝,5,6,63,8,9,93,10,1〇3,1013,11,12-十四氫-7-»号-8-吖-戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟曱基酯 81 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二曱基-2-側氧基-8-(5-曱基-噻吩-2-基曱 基)-2,4&,413,5,6加,8,9,93,10,1(^,101),11,12-十四氮-7-口号 -8-。丫-戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基酯 82 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-8-(4-甲氧基-苄基)-4a,6a-二曱基-2-側氧基 -2,4\41>,5,6,6&,8,9,93,10,103,101),11,12-十四氫_7-崎-8-吖-戍搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基酯 83 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二甲基-8-(3-甲基-丁基)-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-。号-8-吖-戍搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基酯 84 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環戊基曱 基-4b,12-二氣-5-經基-4a,6a-二甲基-2-側氧; -2,4a,4b55,6,6a,8,9,9a,l〇,l〇a,l〇b,ll512-H- E; 吖-戊搭烯并「2,l-al菲-6b·硫代羧酸S-氟曱基酯 85 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二曱基-2-側氧基-8-(4-丙基-苄 基)-2,4木41),5,6,63,8,9,9\10,1(^,1013,11,12-十四氫-7-崎 -8-。丫-戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟曱基酯 101108588 60 201247697 86 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二甲基-8-(3-甲基-苄基)-2-側氧基 -2,41牝,5,6,6\8,9,9\10,10\101),11,12-十四氫-7-»等-8-α丫-戊搭烯并菲-6b-硫代羧酸S-((S)-氟甲基)醋 87 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 經基_4a,6a-二曱;側氧基-8-(5-氣-0塞吩-2_基-甲 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-口等 -8-吖-戊搭烯并[2,1-al菲-6b-硫代羧酸S-氟曱基酯 88 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二曱基-8-(4-曱基-苄基)-2-側氧基 -2,4\牝,5,6,63,8,9,9木10,10\101),11,12-十四氫-7-崎-8-吖-戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基酯 89 (4aS,4bR,5S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-(4-第三-丁 基-¥基)-4b,12-二‘-5-經基-4a,6a-二甲基-2-側氧基 -2,43,41?,5,6,63,8,9,9&,10,10&,1013,11,12-十四氫-7-口号-8-吖-戊搭烯并『2,1-al菲-6b-硫代羧酸S-氟曱基酯 90 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-(2-苯基硫烧基-乙 基)-2,4\牝,5,6,6屯8,9,9&,10,10\1013,11,12-十四氫-7-口号 -8-n丫-戊搭烯并丨2,1-al菲-6b-硫代羧酸S-氟甲基酯 91 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二曱基-2-側氧基-8-(1-丙基-丁 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7- 口号 -8-。丫-戍搭烯并『2,1-al菲-6b-硫代羧酸S-氟曱基酯 92 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8-(2-苯氧基-乙 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7- 口号 -8-吖-戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基酯 93 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5_經基_4a,6a_二甲墓-2-側氧基-8-(5-氣-0夫喃-2-基-曱 基)-2,41牝,5,6,6\8,9,9&,10,1〇3,101),11,12-十四氫-7-口号 -8-吖-戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟甲基酯 94 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環己基 -4b,12-二氟-5·羥基-4a,6a-二甲基-2-側氧基 -2,4\牝,5,6,6&,8,9,9狂,10,10\1013,11,12-十四氫-7-崎-8-吖-戍搭烯并「2,1-al菲-6b-硫代羧酸S-氟曱基酯 101108588 61 201247697 95 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二敗-5-經墓-4a,6a-二曱基-2-側氧基 -2,4\牝,5,6,6&,8,9,9木10,103,101?,11,12-十四氫-7-»号-8-吖-戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基酯 96 (4aS,4bR,5S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-(4-第三-丁 氧基_:^表)-41),12-二氣-5-經基-4a,6a-二曱基-2-側氧基 2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-崎-8-。丫-戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基酯 97 (4aS,4bR,5S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-(4- 丁氧基-卞基)-4b,12-二氟^ -5-經基-4a,6a-二甲基-2-側氧基 -2,43,41),5,6,63,8,9,93,10,1〇3,1013,11,12-十四氫-7-»等-8-吖-戊搭烯并丨2,1-al菲-6b-硫代羧酸S-氟曱基酯 98 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-4a,6a-二甲基-8-(5-甲基-呋喃-2-基甲基)-2-側 氧基-2,4&,牝,5,6,63,8,9,9\10,1(^,1013,11,12-十四氫-7-崎-8-吖-戊搭烯并丨2,1-al菲-6b-硫代羧酸S-氟甲基酯 99 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二曱基-2-側氧基-(5-曱基硫烧基-σ塞吩-2-基甲基)-2,43,牝,5,6,63,8,9,9屯10,1(^,101),11,12-十四氫 -7-崎-8-吖-戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基酯 100 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-((S)-l-乙基-2-曱基-丙;^)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4&,牝,5,6,6屯8,9,9木10,1(^,101),11,12-十四氫-7-口等-8-。丫-戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟曱基酯 101 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-4a,6a-二甲基-2-側氧基-8·(3,3,3-二氣-丙 基)-2,4&,牝,5,6,6\8,9,93,10,103,101),11,12-十四氫-7-口号 -8-吖-戊搭烯并[2,l-al菲-6b-硫代羧酸S-氟曱基酯 102 (4&8,扑11,58,6&8,6511,938,1(^8,1(^8,128)-8-環丙基甲 基-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4七41),5,6,63,8,9,9屯10,1(^,101),11,12-十四氩-7-口等-8-。丫-戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟曱基酯 103 (4&8,处11,58,638,6511,938,1〇35,1(^8,128)-8-(2-環己基-乙基)-4b,12-二氟j -5-經基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-口等-8-吖-戍搭烯并f2,l-al菲-6b-硫代羧酸S-氟曱基酯 101108588 62 201247697 104 (4&3,扑11,58,638,6511,9&8,1(^8,1008,123)-8-二環[2_2.1] 庚-2-基-4b,12-二說-5-經基-4a,6a-二_基-2-側氧基 _2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-«等-8-吖-戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基酯 105 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二甲基-8-((S)-l-甲基-1H-吲哚-3-基-曱基)-2-側氧基-2,4&,415,5,6,6\8,9,9七10,1(^,101),11,12-十四氫 -7-»等-8-吖-戍搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基酯 107 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-氣-乙酿墓)-5-經;^-4a,6a-二甲基-8-(4-曱基-节 基)-4a,4ί),5,6,6a,6ί),8,6,9a,10,10a,10b,ll,12-十四氫j-哼-8-吖-戊搭烯并『2,l-al菲-2-酮 108 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-說-乙酿墓)-5-經基-4a,6a-二曱基-8-0塞吩-2-基曱 -4a,4b,5,6,6a,6b,8,9,9a, 10,l〇a, 10b, 11,12--f- va -8-吖-戊搭烯并丨2,l-al菲-2-酮 109 GaSAbR^SAaS/bR^aSaOaSJObS’US)-^,^·二說 -6b-(2-氟-乙醯基)-8-(4-氟-苄基)-5-羥基-4a,6a-二曱基 -4a,4b,5,S,6a,6b,8,9,9a,10,10a,10b,11,12-十四氫-7-°号Αν-戊搭烯并丨 2,l-al 菲-2-酮 110 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-氣-乙酿;^·)-8-β夫喃-2-基甲基-5-經基-4a,6a-二曱 基-4&,扑,5,6,63,615,8,9,93,10,1〇3,101),11,12-十四氫-7-口号 -8-吖-戊搭烯并「2,l-al菲-2-酮 111 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-氟-乙醯基)-5-羥基-8-(4-甲氧基-苄基)-4a,6a-二 甲基-4&,413,5,6,63,61),8,9,93,10,1(^,1013,11,12-十四氫-7-碍-8-。丫-戊搭烯并丨2,l-al菲-2-酮 112 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-環戊基甲 基-4b,12-二氣-6b-(2-氣-乙酿經基-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10li,l 1,12-十四氫-7-°号-8-吖-戊搭烯并『2,l-al菲-2-酮 113 GaSAbRJSAaSjbR^aSJOaSJObKnSH-aS-二甲 基-丁基)-4b,12-二氟/*6b-(2-氣-乙酿;^)-5-經基-4a,6a-二 曱基-4&,415,5,6,6&,615,8,9,9&,10,1(^,101),11,12-十四氫-7-谔-8-吖-戊搭烯并f2,l-al菲-2-酮 101108588 63 201247697 114 (4aS,4bR,5S,6aS,6bR,9aS,1 OaS,1 ObS,1 -2-基曱墓)-4b,li·二說-6έ)-(2-ίt-乙酿基5_5-經基-4a,6a- 二曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10l3,ll,12-十E^氫 -7-。等-8-。丫-戊搭烯并丨2,1-al菲_2-酮 116 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12·二故 -5-羥基-6b-(2-羥基-乙醯基)-8-[4-(2-羥基-乙氧基)-苄 基]-4a,6a-二曱墓-4a,4b,5,6,6a,6b,8,》,9a,10,10a,ii)b,ll, 12-十四氫-7-。等-8-吖-戊搭烯并丨2,l-al菲-2-酮 122 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-苯基 _4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,11,12-十四氫-7-0等-8-吖-戊搭烯并丨2,l-al菲-2-酮 123 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基·乙醯基)-4a,6a-二甲 基-4\41>,5,6,63,615,8,9,9木10,103,101),11,12-十四氫-7-。号 -8-吖-戊搭烯并丨2,1-al菲-2-酮 124 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-對-甲苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-。等-8-吖-戊搭烯并「2,l-al菲-2-酮 125 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-喹啉-6-基 _4a,4b,5,6,6a,6b,8,9,9a,10,1 Oa,1 Ob, 11,12-十四氫-7-口咢-8· 吖-戊搭烯并丨2,l-al菲-2-酮 126 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b<2-羥基-乙醯基)-4a,6a-二甲基-8-吡啶-3-基 -4a,4b,5,6,6a,6b,8,9,9a,10,1 Oa,10b,11,12-十四氫-7-。等-8-戊搭烯并丨2,l-al菲-2-酮 127 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-間-曱苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-。等-8-»丫-戊搭烯并『2,1-al菲-2-酮 128 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-8-(4-氟-苯基)-5-羥基-6b-((S)-2-羥基-乙醯基)-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,1 Oa,10b,11,12-十四氫-7·« 等-8· 吖-戍搭烯并丨2,1-al菲-2-酮 129 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣·苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱 基-4&,物,5,6,63,613,8,9,93,10,1(^,1013,11,12-十四氫-7_口号 -8-吖-戊搭嫌并『2,1-al菲-2-酮 101108588 64 201247697 130 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(4-三氟甲 基-苯基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+ra 氫-7-冬8-吖-戍搭烯并「2J-al菲-2-酮 131 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-8-(3-氟-苯基)-5-羥基-6b-((S)-2-羥基-乙醯基)-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12·十四氫-7-»等-8-吖-戊搭烯并「2,l-al菲-2-酮 132 WaS/bR^S/aS/bR^aSJOaSJObSJSSHbM-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-鄰-甲苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-崎-8-吖·戊搭烯并丨2,l-al菲-2-酮 133 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-(4-氣-3-甲基-苯基)-4b,12-二氟-5-羥基-6b-((S)-2-羥基-乙醯 基)-4a,6a-二曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll, 12-十四氫-7-»等-8-吖-戊搭烯并「2,l-al菲-2-酮 134 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-3-三 氣曱基苯基)-4b,1二氣經基_6b-(2-經墓-乙酿 基)-4a,6a-二甲基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll, 12-十四氫-7-"等-8-吖戊搭烯并「2,l-al菲-2-酮 135 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,4-二氣-苯基)-4b,12-二政-5-經基-6b-(2-經乙酿基)-4a,6a-二 甲基-4&,413,5,6,63,61),8,9,9&,10,1〇3,1013,11,12-十四氫-7-4-8-吖-戊搭烯并[2,1-al菲-2-酮 136 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-溴-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱 基-4\41),5,6,6&,613,8,9,93,10,1〇3,101),11,12-十四氫-7-口等 -8-吖-戊搭烯并丨2,1-al菲-2-酮 137 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS)-4b-氟 _5_ 羥基 -6b-(2-羥基·乙醯基)-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,l 1,12-十四氫-7-»等-8-吖-戊搭烯并「2,l-al菲-8-基1-苯甲腈 138 4-[(4aS,4bR,5S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-4b, 12-二 氣-5-經基-6b-(2-經基-乙酿基)-4a,6a-二甲基-2-侧氧基 -2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,l 1,12-十四氫-7-»号-8-吖-戍搭烯并丨2,l-al菲-8-基1-笨甲醯胺 139 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b_(2-羥基-乙醯基)-4a,6a-二甲基-8-(4-三氟甲 氧基-苯基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,11,12-十 四氫-7』等-8-吖-戊搭烯并丨2,l-al菲-2-酮 101108588 65 201247697 140 甲烷磺酸 4-[(4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-413,12-二氣-5-經基-613-(2-經基-乙酿;^)-43,6&-二曱基-2-側氧基-2,4〜415,5,6,6461),9,9屯10,10屯101),11,12-十四氫 ·7·«等_8-十戊搭烯并丨2,l-al菲-8-基1-笨基酯 141 (4珏8,扑11,53,638,6匕11,9&8,1〇38,1(^8,128)-8-(4-環己基-苯基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲 基-43,413,5,6,知,61),8,9,9&,10,1〇3,101),11,12-十四氫-7-崎 -8-吖-戊搭烯并丨2,l-al菲-2-酮 142 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-(4-°塞吩-2-基 苯基)-4&,牝,5,6,6^613,8,9,93,10,1〇3,1013,11,12-十四氫-7-。等-8-吖-戊搭烯并「2,l-al菲-2-酮 143 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5 -經墓_6b-(2_經基乙酿基)-4a,6a-二曱基-2-側氧基 -2,4屯41?,5,6加,613,9,9木10,10屯1015,11,12-十四氫-7-«等-8-吖-戍搭烯并『2,l-al菲-8-基1-笨曱酸曱基酯 144 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2·羥基-乙醯基)-8-(4-甲烷磺醯基-苯基)-4a,6a-二甲基-43,41?,5,6加,613,8,9,93,10,1(^,1013,11,12-十四氫 -7-4-8-吖-戍搭烯并「2,l-al菲-2-酮 145 3-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經墓-6b-(2-經墓-乙酿基)-4a,6a-二甲基-2-侧氧墓 -2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,il,12- + 四氫-7- 〇等 -8-"丫-戍搭烯并【2,l-al菲-8-基1-笨甲腈 146 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-輕·基-6b-(2-經基-乙酿基)-4a,6a-二曱基-2-側氧基 -2,4屯41),5,6,6&,61),9,93,10,10&,101),11,12-十四氫-7-»号-8-。丫-戊搭烯并丨2,l-al菲-8-基1-笨墙醯胺 147 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-環丙基-苯基)-4b,12-二氟-5-羥基-6b-(2·羥基-6醯基)-4a,6a-二甲 基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氩-7-»等 -8-。丫-戍搭烯并丨2,l-al菲-2-酮 148 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-丁 基-苯基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-43,41),5,6,6&,615,8,9外,10,10木101?,11,12-十四氫 •7-埒-8-吖-戊搭烯并丨2,l-am-2-酮 149 N-{4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,ll,12-十四氫-7-^-8-吖-戌搭烯并丨2,1-al菲-8-基1-笨基)-曱醯胺 150 (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS, 1 ObS,12S)-4b,12·二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(3-三氟甲基-苯基)-43,牝,5,6加,61),8,9,9&10,1(^,101?,11,12-十四氫-7-碑-8-。丫-戊搭烯并「2,l-al菲-2·酮 101108588 66 201247697 151 GaSebRjSAaS^bR^aSaOaSJObS’US)-^,^-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(3-三氟曱氧基 -苯基)-4^41),5,6,63,61),8,9,93,10,10&,1013,11,12-十四氫-7· 噚-8-吖-戊搭烯并『2,l-al菲-2-酮 152 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-溴-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4日,41),5,6加,61),8,9,9&,10,1(^,1013,11,12-十四氫-7-哼-8-吖-戍搭烯并「2,l-al菲-2-酮 153 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并噻唑-6-基_4b,l2_二氟·5_經墓-6b-(2_經基-乙醯墓)-4a,6a-二甲基 -4&,41),5,6,63,615,8,9,93,10,1(^,101>,11,12-十四氫-7-〇等-8-吖-戍搭烯并丨2,1-al菲-2-酮 154 (4壮3,扑11,58,638,65民9&8,1(^8,1(^8,128)-41),12-二氟-5-經基-6b-(2-經基-乙▲基)-8-(4-經基-苯墓三氣曱烧橫酸 ^艮)-4a,6a-二甲基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12 -十四氫-7-»等-8-吖-戊搭烯并丨2,l-al菲-2-酮 155 GaS^bRjS^aS'bR^aS’lOaSJObS’USW-p-環丙基 苯基)-4b,12-二政-5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱 各-4&,41?,5,6,6&,61),8,9,93,10,1〇3,101),11,12-十四氫-7-口号 -8-吖·戊搭烯并「2,1-al菲-2-酮 156 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 _5-· 經基-6b-(2-經基•乙酿基)-4a,6a-二甲基-8-(4-派咬-4-基 甲基-苯基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12- + ® 氫-7-哼-8-吖-戍搭烯并丨2,l-al菲-2-酮 158 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-》呈基-4a,6a-二甲基-2-側氧基-8-笨基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-0号-8-0丫 -戊搭烯并f2,l-al菲-6b-羧酸 159 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-笨 基)-4b,12-二‘ -5-經基-4a,6a-二甲基-2-側氧基 _2,4a,4b,5,6,6a,8,9,9a,10,1 Oa,1 Ob,11,12-十四氫-7-0 咢-8-〇丫 -戊搭烯并丨2. Ι-al菲-6b-羧酸 160 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-J 基)-4b,lt-二‘ -5-經基-4a,6a-二甲基-2,側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-»号-8-0丫 -戊搭烯并丨2.1-al菲-6b-羧酸 161 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟_5_ 經墓_4a,6a·二曱基_2-側氧基 -δ-間-甲苯基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-η号-8-0丫 -戊搭烯并f2.1_al菲-6b-羧酸 101108588 67 201247697 162 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5· 經墓-4a,6a-二曱基-2-側氧基-8-鄰-曱苯基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-» 号-8-吖 -戊搭稀并f2,l-al菲-6b-叛酸 163 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-對-甲苯基 _2,4a,牝,5,6,6a,8,9,9a,10,10a,1 Ob, 11,12-十四氫-7-口咢-8-吖 -戊搭烯并『2,l-al菲-6b-羧酸 164 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-» 等-8-吖 -戊搭烯并丨2,1-al菲-6b-羧酸 165 (4aS,4bR,5S,6aS 56bR,9aS, 1 OaS, 1 ObS, 12S)-4b, 12-二氟 -8-(4-說-苯基)-5-經基-4a,6a-二曱基-2-側氧基 _2,4a,4b,5,6,6a,8,9,9a, 10,10a,10b,11,12-十四氩-7-哼-8-吖 -戊搭烯并「2,1-al菲-6b-羧酸 166 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-—甲基-2-側氧基-8-。比0定-3-基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,1 Ob,11,12-十四氩-7-。等-8-吖 -戊搭烯并丨2,l-al菲-6b-羧酸 167 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(3-敗-本基)-5-經基-4a,6a-二甲基-2-側氧無· -2,4a,4b,5,6,6a,8,9,9a,10,10a, 10b,11,12-十四氫-7-崎-8-吖 -戊搭烯并「2,1-al菲-6b-羧酸 168 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經基-4a,6a-二曱;-2-側氧基-8-(4-二氣曱基-苯 基)-2,43,41),5,6,63,8,9,93,10,1(^,1013,11,12-十四氫-7-口等 -8-吖-戊搭烯并丨2,l-al菲-6b-羧酸 169 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-苯基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-» 咢-8-吖 -戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟曱基酯 170 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二 ^ -5-經基-4a,6a-二甲基-2-側氧▲ -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,U,12-十四氫-7-崎-8-吖 -戍搭烯并『2,l-al菲-6b-硫代羧酸S-氟曱基酯 171 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基-8-間-曱苯基 -2,4\41),5,6,63,8,9,9&10,10木101),11,12-十四氫-7-口号-8-吖 -戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟曱基酯 101108588 68 201247697 172 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基-8-鄰-甲苯基 _2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-« 咢-8-吖 -戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟甲基酯 173 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基-8-對-甲苯基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l U2-十四氫-7-。号-8-吖 -戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基酯 174 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-崎-8-吖 -戊搭烯并[2,1-al菲-6b-硫代羧酸S-氟甲基酯 175 (4&8,扑11,58,6511,933,1{^8,1(»)8,123)-41),12-二氟-8-(4-氟 -苯基)-5-經基-4a,6a-二曱;-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-« 等-8-吖 -戊搭烯并丨2,l-al菲-6b-硫代羧酸S-((S)-氟曱基)醋 176 (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-4b,12-二氟-5-經喜· -4a,6a-二曱基-2-側氧基-8- 0比咬-3-基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-« 等-8-吖 -戍搭烯并「2,1-al菲-6b-硫代羧酸S-氟甲基酯 177 (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-8-(3-氟 -苯基)-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-°咢-8-吖 -戌搭烯并『2,1-al菲-6b-硫代羧酸S-(⑸-氟甲基)醋 178 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5· 羥基-4a,6a-二甲基-2-側氧基_8-(4-三氟甲基-苯 基)-2,4\41),5,6,6&,8,9,9\10,1(^,101),11,12-十四氫-7-口号 -8-吖-戊搭烯并f2,l-al菲-6b-硫代羧酸S-氟甲基酯 179 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-氣·乙酿基)-5-經基_4a,6a-二甲基-8-苯i -4\41?,5,6,6&,613,8,9,9&,10,1(^,1013,11,12-十四氫-7-崎-8-口丫-戍搭稀并[2,1-al菲-2-嗣 180 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氣-6b-(2-氣-乙酿基)-5-經基-4a,6a-二曱基 -43,牝,5,6,6\61),8,9,93,10,1(^,101»,11,12-十四氫-7-哼-8-吖-戊搭烯并丨2,l-al菲-2-酮 101108588 69 201247697 181 曱烷磺酸 2-[(4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-(4-氣苯基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氣基 _2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-。咢-8-吖 -戊搭烯并丨2,l-al菲-6b-基1-2-側氧基-乙基酯 182 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-(2-氯-乙醯 基)-8-(4-氣-苯基)-4b,12-二氟-5_ 羥基-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»等-8-吖-戊搭烯并丨2,1-al菲-2-酮 183 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5·羥基-4a,6a-二甲基-6b-(2-甲基硫烷基-乙醯墓)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,l 01?,11,12-十四氫 -7-崎-8-吖-戊搭烯并丨2,l-al菲-2-酮 184 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,li-二 -5-經表-4a,6a-二曱基-2-側氧; 2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12_ 十四氫-7-口 咢-8-吖 -戌搭烯并「2,1-al菲-6b-叛酸氣曱基硫酯 185 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二 1 ·5-經基_ -4a,6a-二曱基-2-側氧; -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-崎-8-吖 -成搭烯并「2,l-al菲-6b-羧酸環丙基甲基酯 186 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氣-5-經墓-4a,6a-二曱基-2-側氧各 -2,4a,4b,5,6,6a,8,9,9a,10,10a,1 Ob, 11,12_ 十四氫-7-"等-8-吖 -戍搭烯并「2,l-al菲-6b-羧酸氰基甲基酯 187 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-» 等-8-吖 -戊搭烯并「2,l-al菲-6b-羧酸胺基甲醯基甲基酯 188 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-谔-8-吖 -戊搭烯并丨2,1-幻菲-6b-羧酸2,2,2-三氟-乙基酯 189 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氣-5-經;^ -4a,6a-二甲基-2-側氧表 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-"等-8-吖 -戍搭烯并「2,l-al菲-6b-羧酸2-氟-乙基酯 101108588 70 201247697 190 (4aS,4bR,5 S,6aS,6bR,9aS,1 OaS,1 ObS,12S)-8-(4- 基)_4b,li-二氣·5_經墓_4a,6a-二甲基_2-侧氣某 2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-« 号 •戍搭烯并「2,1-al菲-6b-硫代羧酸S-氰基甲基酯 191 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-^77~^ 基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧美 _2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-n 等 -戊搭烯并丨2.1-al菲-6b·硫代羧酸S-(2-氟-乙基)酷 1 192 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-^~r~l: 基>4b,l2-二氯_5·羥基-如加-二曱基_2·側氧美 -2,4木41>,5,6加,8,9,93,10,10屯1013,11,12-十四氫-7-。号-8_$ -戊搭烯并丨2.1-al菲-6b-硫代羧酸S-(2,2,2-三氟-乙其μ 193 (4aS ,4bR,5S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-8-(4-基)-4b,l2-二氯_5_羥基-4a,6a-二甲基_2-側氣美 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫 -戊搭烯并丨2.1-al菲-6b-硫代羧酸S-胺基甲醯基甲其% 194 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-'g~T^~ 基)-4b,12-二政-5-經基-4a,6a-二曱基-2-側氣美 -2伞,413,5,6加,8,9,93,10,103,101),11,12-十四氫-7-。等1$ •戊搭烯并f2.1-al菲-6b-硫代羧酸S-丙-2-炔基酯 1 195 (4aS,4bR,5S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-8-(4-基)-4b,12-二氣-5-經;-4a,6a-二甲基-2-侧氡甚 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-哼Μ -戊搭烯并『2,1-al菲-6b·硫代羧酸S-環丁基酯 1 196 (4aS54bR55S,6aS,6bR,9aS,ldaS,10bS,12S)-8-(4-~XT~Y 基)-4b,12-二 ‘ -5-經墓-4a,6a-二曱基-2-側氣 | _2,4&,41),5,6加,8,9,93,10,1(^,1013,11,12-十四氫-7-<1等$·^ -戍搭烯并「2,1-al菲-6b-硫代羧酸S-(2-側氧基-丙甚袖 197 (4aS,4bR,5S,6aS,6bR59aS,10aS,10bS,12S)-8-(4-基)-4b,12-二^ -5-經基-4a,6a·二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氮-7-0 号-8-。丫 -戊搭烯并丨2,1-al菲-6b-羧酸曱基酯 198 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧墓 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,l 1,12-十四氫-7-»等-8-吖 -戊搭烯并丨2,l-al菲-6b·羧酸氡某甲某-甲篡-醯胺 101108588 71 201247697 199 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二▲ -5-經;-4a,6a-二曱基-2-側氧墓 _2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7·» 咢-8-吖 -戊搭烯并丨2,1-al菲-6b-硫代羧酸S-甲基酯 201 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-乙醯基 -8-(4-氣-苯基)-4b,12-二氣-5-經基-4a,6a-二甲基 -4\41),5,6,63,613,8,9,93,10,1(^,1013,11,12-十四氫-7-'»等-8-吖-戊搭烯并丨2,l-al菲-2-酮 202 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二^ -5-經墓-4a,6a-二曱基-2-側氧墓 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-崎-8-吖 -戊搭烯并「2,l-al菲-6b-羧酸1,1-二甲基-丙-2-炔基酯 203 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氣-5-經墓-4a,6a-二曱基-2-側氧墓 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,11,12-十四氫-7-»等-8-吖 -戊搭烯并「2,l-al菲-6b-羧酸1,1-二甲基-熵丙基酯 以實例中所述類似程序獲得的其它較佳通式⑴化合物為 下列: _化學名稱__ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二甲基-2-側氧墓-8-(3-苯基-丙基)-i,4a,4b,5,6,6a, 8,9,93,10,1(^,1013,11,12-十四氫-7-»号-8-。丫-戊搭稀無[2,1-3] 菲-6b-羧酸二甲基醯胺 (4aS,4bRJ5S,6aS,6bR59aS,10aS,10bS,12S)-8-(3,3-ji- f 基)-4b,12-二氟-5-羥基-4a,6a-二甲基·2·側氧基 -2,4丑,413,5,6,63,8,9,9&,10,1(^,101?,11,12-十四氫-7-»等-8-〇丫- 戊搭烯并丨2,1-al菲-6b-羧酸4基甲基醋___ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12- 一'氣-6b-(2-氣-乙▲基)-5-經基-4a,6a-二曱基 -4&,413,5,6,63,615,8,9,93,10,10&,101>,11,12-十四氫-7-<«等-8-吖- 戊搭烯并「2.1-al菲-2-酮__ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氣-5-經 | -4a,6a-二曱基-2·側氧基-8-(3-苯基-丙 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-谔各 Ltil^4I^hil||^IJ^iiϋJJ|__ 依據本案所述類似程序及方法,可獲得由下表報告之本 發明之較佳化合物: 101108588 72 201247697 _化學名稱_ (4&8,朴11,58,633,6511,9&8,1(^8,1053,128)-413,12-二氟-5-羥 基 -4a,6a- 二甲基 -Ί- 側氧基 -8- 丙基 -2,4&,41?,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-。等-8-吖- 戊搭烯并『2,1-al菲-6b-硫代羧酸S-氟曱基醋_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二甲墓-2-側氧基-8-。比。定-3-基 -2,4&,朴,5,6,63,8,9,93,10,1(^,1013,11,12-十四氫-7-哼-8-吖- 戊搭烯并[2,l-al菲-6b-硫代4酸S-氟甲基醋_ (4&8,牝11,58,6&8,6511,938,1〇38,1(^8,123)-413,12-二氟-5-羥 基-4a,6a-二曱墓-2-側氧基-8- D塞。坐-4-基 -2,43,41?,5,6,6&,8,9,9&,10,1〇3,101),11,12-十四氫-7-。等-8-吖- 戊搭烯并[2,1-al菲-6b-硫代4酸S-氟甲基醋_ (4已8,仆11,58,6&8,6511,9&3,1{^3,1(^8,123)-413,12-二氟-5-羥 基-4a,6a-二曱基-8- 哇-2-基-2-側氧基 -2,4&,41),5,6,6&,8,9,9玨,10,103,1013,11,12-十四氫-7-»号-8-吖- 戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基醋_ (4巳8,牝11,58,638,6511,938,1(^8,1(^8,128)-413,12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-噻唑-2-基曱基 -2,4&,413,5,6,63,8,9,9&,10,1〇3,1015,11,12-十四氫-7-崎-8-吖- 戊搭烯并丨2,l-al菲-6b-硫代4酸S-氟甲基酿_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-5j:i 基-8-(2-咪唑-卜基-乙基)-4a,6a-二甲基-2-側氧基 -2,4&,朴,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-崎-8-吖- 戊搭烯并Ρ,Ι-al菲-6b-硫代4酸S-氟甲基醋_ (4&3,仆11,58,6&8,6511,9&8,1(^8,1(^8,123)-413,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(3- 0比0定-3-基-丙 基)-2,4&,41>,5,6,6&,8,9,93,10,1(^,1(^,11,12-十四氫-7-»号-8- p丫-戍搭知弁「2,l-a~| -6b-硫代叛酸S-氟曱基酉旨_ (438,仆11,58,6&8,6511,938,1〇38,1{^3,128)-仆,12-二氟-8-呋 0南-3-墓-5-經墓-4a,6a-二曱基-2-側氧基 -2,4&,41?,5,6,63,8,9,9玨,10,103,1013,11,12-十四氫-7-崎-8-吖- 戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基酷_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5jf 基-8-(1Η-吲哚-3-基甲基)-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-。号-8-吖-戊搭烯并[2,l-al菲-6b-硫代羧酸S-氟曱基醋_ 101108588 73 201247697 (4&8,仆11,58,633,6511,933,1〇83,1(^8,128)-413,12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-啥琳-7-基甲基 -2,43,41>,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-。号-8-吖- 戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基醋_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并噻唑-2-基甲基-4b,12-二乳-5-經基-4a,6a-二曱;-2-側氧基 -2,4&,仆,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-'>等-8-吖- 戊搭烯并丨2,l-al菲-6b-硫代羧酸S-氟曱基酿_ (438,扑11,53,6&3,6511,988,1(^8,1(^3,128)-413,12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-喹啉-5-基甲基 -2,4&,413,5,6,63,8,9,93,10,1(^,1013,11,12-十四氫-7-»等-8-吖- 戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基醋_ (438,牝11,53,6&8,6511,988,10&8,1(^3,123)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-啥琳-2-基甲基 -2,43,41?,5,6,68,8,9,9&,10,103,1013,11,12-十四氫-7-崎-8,吖- 戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基酉旨_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并呋喃-3-基-4b,12-二氯1 -5-經基-4a,6a-二甲基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,103,1013,11,12-十四氫,7-«等-8-吖- 戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基醋_ (438,仆11,53,6&3,6511,938,1(^8,1058,128)-8-苯并[1,3]二 呢-5-基-4b,12-二氣-5-經基-4a,6a-二甲無 -2-側氧基 -2,4&,41),5,6,6日,8,9,9&,10,1〇3,1013,11,12-十四氫-7-今-8-吖- 戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟曱基醋_— (4丑3,牝11,58,6&8,6511,988,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二曱基-8-(1-甲基-1H-吲哚-2-基)-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫·7-α 等-8-吖- 戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基醋_ (4&8,仆11,53,6&8,6511,938,1〇38,1058,123)-415,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(1-曱基-1H-吲哚-3-基曱 基)-2,4&,41?,5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7-崎-8- 吖-戊搭烯并「2,l-al菲-6b-硫代羧酸S-氟甲基醋_ (4&3,仆11,53,6&8,牝11,938,1(^3,1(^8,123)-41?,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(1-甲基-1H-咪唑-4-基甲 基)-2,4&,413,5,6,63,8,9,93,10,1(^,1013,11,12-十四氫-7-»号-8- 吖-戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基醋_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5〇i 基-8-(1Η-咪唑-2-基曱基)-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-« 等-8-吖- 戊搭烯并『2,l-al菲-6b-硫代羧酸S-氟甲基醋_ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-n 等-8-吖-戊搭烯并f2,l-al菲-6b-硫代羧酸S-氟曱基醋_ 101108588 74 201247697 (4&8,扑11,58,6&8,6511,9&8,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8- -曱苯基 -2,4&,415,5,6,6丑,8,9,9&,10,10&,101),11,12-十四氫-7-»等-8-吖- _戊搭烯并丨2,1-al菲-6b-硫代施酸S-氟甲某酷__ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5-· 基_8-(4-甲氧基-苯墓)_4a,6a-二争基-2-側氧基 -2,4牡,415,5,6,63,8,9,9&,10,1〇3,101),11,12-十四氫-7-°咢-8-吖- 并『2,l-al菲-6b-硫代竣酸S-氟甲某SI__ (如8,仆11,58,6&8,6611,9&8,1(^8,1068,128)-仆,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-鄰-甲苯基 -2,4&,415,5,6,63,8,9,9&,10,10心1015,11,12-十四氫-7-崎-8-吖-__戊搭烯并Γ2,1 -al菲-6b-箱代羧酴S-i.甲基酯 (4&8,仆11,58加8,牝11,9&8,1〇38,1(^8,128)-413,12-二氟-5-羥 基-8-(3_曱氧基苯墓)_4a,6a-二+基_2_側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-*f 四氫-7·«»等-8-吖-i搭烯并【2,l-al菲-6b-硫代4酸S-氟甲某6¾__ 本發明也提供包含本發明化合物或為就此形式或為醫藥 上可接受之鹽及一或多種醫藥上可接受之載劑及/或賦形劑 之醫藥組成物。 本發明化合物也可作為唯一活性劑投藥或組合其它醫藥 活性成分包括目前用於治療呼吸病症的成分投藥,例如β2· 促效劑、抗蕈毒驗劑、皮質類固醇、有絲分裂原活化蛋白 質激酶(Ρ38 MAP激酶)抑制劑、核因子κ_β激酶亞單元 β(ΙΚΚ2)抑制劑、人類嗜中性細胞彈性蛋白酶(ηνε)抑制 劑、磷酸二酯酶4(PDE4)抑制劑、白三烯調節劑、非類固醇 抗發炎劑(NSAID)及黏液調節劑。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 與選自於由下列所組成之組群中之β2-促效劑之組合物:卡 莫特羅(carmoterol)、GSK-642444、英達卡特羅 101108588 75 201247697 (indacaterol)、迷爾維特羅(miiveter〇i)、阿佛莫特羅 (arformoterol)、佛莫特羅(formoter〇i)、沙布塔摩 (salbutamol)、雷法布特羅(levalbuterol)、特布塔林 (terbutaliiie)、AZD-3199、BI-1744-CL、LAS-100977、邦布 特羅(bambuterol)、埃索波特諾(iSOpr〇terenol)、波卡特羅 (procaterol)、克蘭布特羅(cienbuterol)、瑞波特羅 (reproterol)、菲諾特羅(fen〇ter〇l)及ASF-1020及其鹽。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 與選自於由下列所組成之組群中之抗蕈毒驗劑之組合物: 阿克迪寧(aclidinium)、提歐徹平(tiotropium)、伊帕徹平 (ipratropium)、徹斯平(trospium)、葛皮若寧(glycopyrronium) 及歐喜徹平(oxitropium)鹽。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 與選自於由下列所組成之組群中之PDE4抑制劑: AN-2728、AN-2898、CBS-3595、阿沛米雷(apremilast)、 ELB-353、KF-66490、K-34、LAS-37779、IBFB-211913、 AWD-12-281 、喜潘菲林(cipamfylline)、喜洛米雷 (cilomilast)、洛芙米雷(roflumilast)、BAY19-8004 及 SCH-35159卜 AN-6415、indus-82010、TPI-PD3、ELB-353、 CC-11050、GSK-256066、歐格米雷(oglemilast)、OX-914、 特托米雷(tetomilast)、MEM-1414及RPL-554。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 101108588 76 201247697 與選自於由下列所組成之組群中之p38 MAp激酶抑制劑:塞 麻皮莫(semapimod)、妥瑪皮莫(taimapim〇d)、頗菲尼東 (pirfenidone)、PH-797804、GSK-725、米諾金(minokine)及 洛瑪皮莫(losmapimod)及其鹽。 於較佳具體例中,本發明提供發明化合物與IKK2抑制劑 之組合物。 本發明也提供發明化合物與選自於由下列所組成之組群 中之ΗΝΕ抑制劑之組合物:ΑΑΤ、ADC-7828、亞瑞法 (Aeriva)、TAPI、ΑΕ-3763、KRP-109、AX-9657、P〇L_6014、 AER__002 ' AGTC-0106、瑞斯皮法(reSpriva)、AZD-9668、 哲麥拉(zemaira)、ΑΑΤ IV、PGX-100、伊拉芬(eiafin)、 SPHD-400、前彈性蛋白(pr〇iastin)c及吸入型前彈性蛋白。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 與選自於由蒙特露孰(montelukast)、哲菲露凯(zafiriukast) 及潘露凱(pranlukast)所組成之組群之白三烯調節劑。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 與選自於由下列伊布波芬(ibuprofen)及凱托波芬(ketoprofen) 所組成之組群中之NSAID。 本發明也提供發明化合物本身或呈醫藥上可接受之鹽, 與選自於由下列1奶-37217、迪夸佛索((^1^〇3〇1)、席貝拿 堆(sibenadet)、CS-003、妥内坦(talnetant)、DNK-333、 MSI-1956及吉菲特尼(gefitinib)所組成之組群中之黏液調節 101108588 77 201247697 劑。 本發明也提供發明化合物用作為藥物。 本發明也係有關於發明化合物用於試管内及/或活體内減 少發炎細胞數目、活性及移動。 本發明也係有關於發明化合物用於其中涉及減少發炎細 胞之數目、活性及移動之任何疾病的預防或治療。 於又一態樣中,本發明提供發明化合物用於其中涉及減 少發炎細胞之數目、活性及移動之任何疾病的預防及/或治 療之用途。 疾病 更明確言之,本發明化合物或為單獨使用或組合一。、夕 種活性成分可投予用於以呼吸道梗阻為特徵的、、或夕 諸如氣喘及COPD之預防及/或治療。 ^ 物製備之 活性及移 於又一態樣中,本發明提供發明化合物用於藥 用途’該藥物係用於其中涉及發炎細胞之數目、、 動減低之任何疾病的預防及/或治療。 活性 此外’本發明提供其中涉及減少發炎細胞之數目 及移動之任何疾病的預防及/或治療之方法,誃、 有需要此種治療之病人投予治療上有欵 匕&對 物 <本發明化合 口服或鼻内投藥之本 進劑之定量噴霧劑或 本發明也提供適合藉吸入、注射、 發明化合物之醫藥製劑。 吸入性製劑包括吸入性粉末、含推 !〇Π〇8588 ηο 201247697 不含推進劑之吸入性配方。
物之軟霧喷霧器。
本發明化合物可依據多個合成步驟製備,該等步 據習知方法及技術進行或後文說明之方法或技術進行。、 於-個紐巾,本發明提供本發明化合物及其^產物 之製備方法。 本發明也係有關於一種通式(1,)化合物之製備方法,其中 Κ(:Η2)η-Ζ-((:Η2)η’-Κ3,n及n’=〇,2及尺3係如前文定義, 該方法包含將通式(VI)化合物於位置6|3之2_羥基乙醯基部 分的羥基轉換成通式(XI)化合物之離去基(LG)
其中LG可由親核基團置換或其中於將lg導入C21羥基部 分上之後,可進行氧化還原反應來獲得相對應之曱基甲酮。 本發明也係有關於通式(Γ)化合物之製備方法,其中R1 = 101108588 79 201247697 -(CH2)n-Z-(CH2)n,_R3 ’ n及n’=〇 ’ Z及R3係如前文定義,該方 法包含: -式(VI)化合物反應獲得通式(XII)化合物
-以一或多當量酸活化劑然後以親核基團處理式(XII)化合 物。 本發明也係有關於通式(Γ)化合物之製備方法,其中心= -(CH2)n-Z-(CH2)n,-R3 ’ n=n’=0 ’ Z=S及R3係如前文定義, 該方法包含: -式(VI)化合物於氧化條件下反應獲得通式(XII)中間產物 -其轉換成通式(XIII)化合物
-式(XIII)化合物之烷化。 本發明也係有關於一種通式(VI)化合物之製備方法
OH
101108588 80 (VI) 201247697 該方法包含: -通式(IV)化合物
與N-四氫哌喃基羥基胺(HO-NH-THP)反應製備式(V)化 合物
-式(V)化合物之選擇性進一步官能化及 -脫去保護。 本發明也係關於一種通式(VI)化合物之製備方法,該方法 包含: -式(VII)化合物
與式(X)化合物反應
本發明也係關於一種通式(VI)化合物之製備方法,該方法 101108588 81 201247697 包含: -式(VII)化合物與N-四氫哌喃基經基胺(Η0·丽_THP)反 應獲得式(νιπ)化合物
-保護式(VIII)化合物獲得式(Ιχ)化合物
-式(IX)化合物選擇性地進一步官能化及 -脫去保護。 本發明也係有關於通式(][,)化合物之製備方法,其中R1 = -(CH2)n-Z-(CH2)n’-R3,ϊ^η,=〇,z = 〇及r3 = Ac,該方法包 含通式(IV)中間產物與式(X)羥基胺反應。 本發明也係有關於通式(1,)化合物之製備方法,其中r1 = -(CH2)n-Z-(CH2)n,-R3,n=〇,n,=p r3 = f,該方法包含 -化合物(VII)與曱烷磺醯氣及dipea於無水乙腈反應; -氟化四正丁基銨(TBAF)與KI之原位加成反應,及 •所得中間產物(XV)與HO-NH-THP之環化加成反應 101108588 82 201247697
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本發明也係有關於通式(Γ)化合物之製備方法’其中R1 = _(CH2)n-Z-(CH2)n,-R3,n=l,n’=0,Z=0,R3 = H及X=C1 如反應圖報告,該方法係經由式(I’)化合物其中n=l,n’=0 ’ Z=0,R3 = Ac及X = H與曱烷磺醯氯於鹼存在下反應獲得式 (XIV)化合物
該化合物與氯化劑反應及於藉鹼處理而水解乙醯基酯後 獲得前述通式(Γ)化合物。 於本發明之難具體财,全部前线明之方法皆係使 用此處X及Y為氟之化合物及中間產物進行。 由全部前文說明,熟諳技藝 適當立體化學組態之起始物料 構物中之任一者。 如反應圖1所述’若干用 用於式(I)化合物。 熟叫技藝人士顯然易知經由選擇具有 起始物料,可獲得可能的式(I)立體異 干用於製備式(I’)化合物之方法也係適 101108588 83 201247697
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Gvix} 101108588 85 201247697 [本發明化合物之製備程序] 依據特定具體例,本發明化合物可依據反應圖1所述不同 途徑製備,取決於取代基1^及112之本質。 途徑A1-通式(IV)化合物與N-四氫旅π南基經基胺 (ΗΟ-ΝΗ-ΤΗΡ)反應而製備式(V)化合物可方便地於80至 100°C範圍之溫度於質子性溶劑諸如乙醇内進行。ΤΗΡ保護 基可於反應條件下直接裂解。 此等化合物更進一步使用習知方法(J. Med. Chem·, 379-388,1995 ; J.C.S. Chem. Comm.,256-257, 1985)以烷基 鹵化物、醯基鹵化物、異氰酸酯類、胺曱醯氣類或磺醯氣類 官能化獲得通式(VI)化合物。此等反應通常係於溶劑如二氣 曱烷(DCM)或四氫呋喃(THF)及於室溫(RT)至回流溫度範圍 之溫度進行。鹼諸如三乙基胺或二異丙基乙基胺可能需要來 促進反應。與芳基函化物之反應可於已知銅催化異崎唑啶之 N_芳基化下進行(Bioorg. Med. Chem. Lett.,2834, 2005)。乙 醯基酯容易使用醇類脫去乙醯基之標準條件水解,例如使用 鹼如氫氧化鈉或氫氧化鉀或碳酸鉀於適當溶劑(例如曱醇或 乙醇)處理該化合物。本反應通常係於室溫進行1至5小時時 間,結果導致獲得通式(VI)化合物。 通式(IV)化合物可方便地依據參考文獻報告之標準程序 製備。例如可經由使用鹼如乙酸鉀處理通式(III)化合物製 備。本反應通常係於適當極性溶劑諸如二曱基甲醯胺(DMF) 101108588 86 201247697 中及典型地於80至110°C範圍之溫度進行經歷0.5至4小時時 間。 式(III)化合物方便錯已知方法,始於通式(II)化合物而從 已知化合物製備(J. Med. Chem. 1982, 25, 1492-1495)。 途徑A2-另外,通式(VI)化合物可藉硝酮之環化加成,使 用異哼唑啶形成之已知程序,始於式(VII)化合物與式化 合物於三聚甲醛存在下反應而製備(J. Med. Chem.,25, 1492-1495,1982)。反應方便地於質子產生性溶劑諸如乙醇 於80至100°C範圍之溫度進行。式(X)羥基胺為市售可得或可 使用熟諳技藝人士眾所周知之程序容易地製備,例如經由使 用還原劑諸如硼烷吡啶錯合物還原肟(j. Med. Chem” 40, 1955-1968,1997)或經由〇-四氫哌喃基羥基胺與適當烷化劑 諸如烧基鹵反應而製備(Chem. Pharm. Bull.,46, 966-972,1998) 〇 式(VII)化合物可水解式(ιν)化合物製備。本反應可經由化 合物(IV)接受_諸如得自南極念珠菌(Candida Antarctica)之 制動月曰解 (Sigma Aldrich)的作用進行(Tetrahedron,50, 13165-13172,1994) 〇 途徑A3_通式(VIII)化合物可始於式(VII)化合物與 HO-NH-THP反應製備。本反應可方便地於二崎4或於質子 性溶劑諸如乙醇於8〇。(:至100。(:範圍之溫度進行^ THP保護 基可於反應條件下直接裂解。所得(νπι)可經由使用二氫哌 101108588 87 201247697 喃於適當溶劑諸如DCM或THF於0°C至室溫之溫度處理而方 便地選擇性地保護來獲得式(ιχ)化合物。反應係於0.5至3小 時範圍之時間完成。式(IX)化合物可如途徑Α1所述進一步使 用燒基鹵、醯基鹵、異氰酸酯、胺基甲醯氯或磺醯氯官能化。 ΤΗΡ保護基容易經由使用鹽酸於適當溶劑諸如THF或二谔 °山處理經保護之中間產物而去除。此反應通常係於室溫進行 1至15小時時間結果獲得通式(VI)化合物。 途徑Α-通式(VI)化合物於位置6b之2-羥基乙醯基部分之 羥基轉成通式(XI)化合物之離去基(LG)可經由使用曱烷磺 醯氣或對曱苯磺醯氯處理式(VI)化合物進行(March之 「Advanced Organic Chemistry」,Wiley-Interscience),該反 應係於適當溶劑諸如吡啶進行。此反應通常係於室溫進行l 至5小時時間。 通式(XI)化合物之LG方便藉親核基團諸如鹵陰離子、醇 類、硫醇類、硫代酸類、胺類、醯胺類及碳陰離子置換(J. Org. Chem., 1042, 1999 ; J. Steroid. Biochem. 13, 311-322,1980) 而獲得通式(I)及(Γ)化合物其中Ι^ = -((:Η2)η-Ζ-((:Η2)η,·Ι13,n 及n’=0,乙及尺3係如前文定義。反應通常係於適當溶劑諸如 DCM、THF或DMF於0至80°C範圍之溫度經歷1至5小時時間 進行,該反應可藉鹼諸如碳酸鈉或碳酸鉀或氫化鈉促進。於 將LG(例如曱烷磺酸根)導入C21羥基部分上時,例如可利用 過量碘化鈉進行氧化還原反應來獲得相對應之曱基酮。所得 101108588 88 201247697 產物可進一步經官能化修改藉前述親核取代反應所導入的 部分。 途徑B-於眾所周知之氧化條件下式(VI)化合物反應獲得 通式(XII)中間產物β本反應通常係於開放空氣中於室溫歷 經12至48小時時間’於適當溶劑諸如THF於無機鹼水溶液諸 如氫氧化納或氫氧化卸存在下進行。 途徑B1-式(XU)中間產物轉成通式⑴及(1,)化合物其中 = -(CH2)n-Z_(CH2)n’-R3,η及n’=0,Z及R3係如前文定義之轉 化反應係經由使用一或多當量酸活化劑諸如甲醯基二咪唑 或HATU處理酸(χπ)。反應通常係於適當極性溶劑如dmf於 0至80 C範圍之溫度歷經1_2小時時間進行。活化酸可與親核 基團諸如醇類、硫醇類、硫代酸類及胺類反應。反應可由鹼 諸如碳酸鈉或碳酸鉀、氫化鈉促進及於〇至2〇充範圍之溫度 進行1至24小時時間。 另外’式(XII)中間產物可於眾所周知之條件下,使用草 醯氯於適當溶劑如DCM轉成相對應之醯基氯。活性中間產 物可與親核基團諸如醇類、硫醇類、硫代酸類、胺類及碳陰 離子諸如烷基、芳基及雜芳基銅酸酯或參考文獻報告之其它 金屬有機化合物反應而將醯基氣適當轉化成為相對應.之酮 類。 式(XII)中間產物也可轉化成通式⑴及(1,)化合物其中Ri== -(CH2)n-Z-(CH2)n’-R3 ’ n及n’=〇,z=〇及R3係如前文定義, 101108588 89 201247697 該轉化係經由使用鹼如碳酸鉀、碳酸鈉或碳酸鉋及三乙基胺 於適當溶劑如DMF或乙腈於〇至20°C範圍之溫度處理酸 (XII)。偶爾此等烧化反應可藉銅鹽諸如峨化銅於KI存在下 促進。所得產物可進一步經官能化修改藉前述親核取代所導 入之部分。 途徑B2-式(XII)中間產物轉化成通式(XIII)化合物,從酸 (XII)與甲醯基二咪唑或HATU反應衍生,接著與硫代乙酸之 鈉鹽或無水硫化氫反應。該反應通常之進行方式係將預先形 成之鹽於反應溶劑之溶液於0至20°C範圍之溫度添加至活化 酸之溶液’或直接添加固體無水硫化氮納。方便形成的硫代 酸衍生物(XIII)係於原位與烷化劑諸如溴烷反應形成,結果 獲得通式⑴及(Γ)之硫酯類,其中R!= -(CH2)n-Z-(CH2)n,-R3,η及n’=0,Z=S及尺3係如前文定義。 適當溴烷諸如溴-氣曱烷之選擇允許式(I)及(Γ)化合物之製 備’其中尺1 = -((1!112)11-7-((11112)1|,-尺3,11及11’=0,2=8及1^3係 如前文定義可更進一步經修改。例如,此等化合物其中R3 為氣曱基與碘化鉀反應,接著使用氟化銀處理,允許製備式 ⑴及(Γ)化合物其中R3=氟曱基。此等反應為熟諳技藝人士 眾所周知(J. Med. Chem·,37, 3717-3729, 1994)。另外,硫代 酸中間產物(XIII)可於原位與溴氟甲烷之DMF溶液反應順利 獲得式(I)及(I,)化合物其中R3=氟甲基。 途徑C-使用藉硝酮之環化加成形成異哼唑啶之已知程 101108588 90 201247697 序,通式(ιν)中間產物與式(x)羥基胺於三聚甲醛存在下反 應。反應可方便地於質子產生性酸諸如乙醇中進行。反應方 便地於高溫例如60至85°C進行及結果獲得通式(I)及(I,)化合 物其中Ri = -(CH2)n-Z,(CH2)n’-R3 ’ 其中n=l,n’=0,Z=0 及R3 = Ac係如前文定義。 通式(XIV)中間產物可經由於鹼諸如吼咬存在下於適當溶 劑諸如DMF使用曱烷磺醯氣處理通式(I)及(I,)化合物其中Rl = -(CH2)n-Z-(CH2)n,-R3 ’ 其中n=l,n,=〇,Z = 〇,R3 = Ac 及X = H而製備。反應係於80至1〇〇。匚範圍之溫度進行i至5 小時時間。 式(XIV)化合物於始於相對應烯於用於製備氣醇之眾所周 知之條件下反應式(XIV)化合物,獲得通式(Γ)化合物其中Ri (CH2)n-Z-(CH2)n’-R3,n= 1,n’=〇,Z= 〇,R3 = Η及X =
Cl係如刖文定義。反應涉及使用氣化劑諸如N-氯丁二醯亞胺 或一氣-5,5-二曱基乙内醯脲,且係藉酸諸如過氣酸促進。反 應通常係於極性溶劑諸如THF於仏耽範圍之溫度經歷】 至4小時時間進行。式(χιν)化合物之乙酿基醋容易地使用醇 之脫乙it化之標準條件水解,使帛驗諸如碳義或碳酸鉀於 办劑諸如甲醇或乙醇處理化合物。此反應通常係於低溫,〇 至2叱範圍之溫度進行〇.5至2小時時間。 途徑D-通式(VI)中間產物與乙酿氯使用已知程序反應。反 應通常係於DCM作為溶劑’於驗諸如三乙基胺存在下於室 101108588 201247697 溫經歷20至50小時時間進行。本程序提供式(1,)化合物其中 ’ η= 1,n’=0,Z=〇,R3係如前文 定義。 途徑E-化合物(VII)與曱烷磺醯氯及Ν,Ν-二異丙基乙基胺 (DIPEA)於無水乙腈反應。然後,氟原子的導入可藉於原位 添加氟化四正丁基銨(TBAF)及ΚΙ及加熱8至20小時時間進 行。所得中間產物(XV)與式(χ)羥基胺於三聚曱醛存在下於 途徑C所述已知條件下之環化加成反應,獲得式(〗,)化合物, 其中 R! _(CH2)n-Z-(CH2)n,-R3,n=G,n’=i,r3 = f 及尺2係 如前文定義。 式(X)經基胺為市售可得或可依據不同合成途徑製備,其 中部分合成途徑為熟諳技藝人士眾所周知。 於本發明之_個態樣中’提供製備式(χ)減胺之合成途 徑如反應圖3所述。 反應圖3
(ΧΪΧ) 途徑G 取代
Ry- ,.ΟΤΗΡ hci/h2o
Ry^V'
(XVIII) % RZ"N、CT
途徑H κΛ (XVI)
途徑F nh2oh hci TEA, DCM
OH (Xa) BH3Py HCI et〇H
(XVII)
<Xb)
途徑L Y、R2 (XXII) 101108588 92 (XXI) 201247697 途徑F-通式(XVI)化合物與羥基胺鹽酸鹽(NH2OH HC1)於 三乙基胺存在下反應製備式(XVII)肟可方便地於DCM作為 溶劑於室溫至50°C範圍之溫度進行。 此等化合物[通式(XVII)肟]可使用還原劑諸如硼烧吼咬錯 合物及HC1於極性質子性溶劑如乙醇於室溫還原成通式(Xa) 羥基胺,其中Rx及Ry於本發明範圍内具有不同定義 (Tetrahedron 1992, Vol. 47, N。17, 3557-3570; J. Med· Chem. 1997, 40, 1955-1968)。通式(XVI)化合物為市售可得或可藉 眾所周知之程序氧化通式(XVIII)化合物獲得(例如Swern oxidation: J.A.C.S.,2005, 127, 29, 10396)。
途徑G-另外,通式(Xa)化合物可經由通式(XIX)之活性化 合物,此處LG為適當離去基,諸如鹵陰離子(C卜Br或I)、 曱烷磺酸根、曱苯磺酸根或其它離去基與0-四氫哌喃基羥基 胺(NH2OTHP)使用眾所周知之程序反應來產生式(XX)中間 產物(J.A.C.S. 2000, 122, 18, 4522; Tetrahedron 1999, 55, 41, 12069),及隨後將THP保護基脫去保護。取代反應方便地於 DMF、乙醇或乙腈作為溶劑於不同種鹼諸如碳酸鉀或DIPEA 及於室溫至80°C範圍之溫度方便地進行。通式(XIX)化合物 可為市售可得或可始於通式(XVIII)醇及藉熟諳技藝人士眾 所周知之程序將羥基轉成適當離去基而製備。例如,曱烷磺 酸酯可方便地得自醇(XVIII)與曱烷磺醯氣及TEA於DCM (Organic Letters 2002, vol. 4, N〇15, 2485)。 101108588 93 201247697 途徑Η-通式(Xb)之羥基胺其中尺2為選擇性地經取代之芳 基或雜芳基’可始於相對應之硝基-芳基化合物或硝基-雜芳 基化合物製備。例如,硝基化合物(XXI)可使用BiCl3及KBH4 於極性質子性溶劑諸如乙醇於室溫方便地還原成為羥基胺 (Synthetic Communications 1997, Vol. 27, Νο20, 3497-3504)。另外,芳基或雜芳基羥基胺(Xb)可方便地經由 使用肼於阮尼鎳存在下於適當溶劑混合物諸如乙醇及二氯 曱烷溶劑混合物内還原硝基化合物(XXI)獲得(Synthesis 1984, 11, 938-941)。於本程序中,需要將溫度控制於〇。〇至 1 〇°C。最後’另一種獲得通式(Xb)化合物之方便還原方法包 含於不同極性溶劑諸如丙酮或乙醇使用鋅及氣化銨還原化 合物(XXI)(Tetrahedron Letters 2005,Vol.46,N。35, 5913-5918; Joe 1982, 47, 7, 1171)。 途徑L-另外,如前文定義之通式(Xb)芳基或雜芳基羥基 胺’可使用熟諳技藝人士顯然易知之方法,經由以羥基胺從 芳基或雜芳基電子欠乏氣化物或氟化物進行親核芳香族取 代而製備。例如通式(XXII)化合物,其中Y為適當離去基諸 如氣或氟與水性羥基胺於乙醇反應(J. Med. Chem. 2009, 52, 19, 5974)可獲得通式(Xb)羥基胺。反應係於回流進行6至10 小時時間》不同方法(WO2006/74187; (2006); (A2)英文)描述 適當芳基或雜芳基電子欠乏氯化物或氟化物與羥基胺鹽酸 鹽於極性質子性溶劑諸如異丙醇反應。該反應可方便地於 101108588 94 201247697 130C溫度微波加熱15至25小時時間β 優異地,本發明化合物可以〇 〇〇1至1〇〇〇毫克/日,較佳〇」 至500毫克/日之劑量投予。 當係藉吸入途徑投藥時,本發明化合物之劑量優異地為 0·01至20毫克/日,較佳為0.1至10毫克/曰。 較佳地’本發明化合物單獨使用或組合其它活性成分可投 予用於任何阻塞性呼吸疾病諸如氣喘、慢性支氣管炎及慢性 阻塞性肺病(COPD)之預防及/或治療。 但可投予本發明化合物用於其中涉及發炎細胞、數目、活 性及移動性減低之任何疾病的預防或治療。 此等疾病之實例包括:涉及發炎之疾病諸如氣喘及其它過 敏病症、COPD、急性鼻炎;逆轉急性移植排斥及急性選擇 性自體免疫病、骨髓移植之植體對宿主病之急性惡化;自體 免疫病諸如類風濕性關節炎及其它關節炎;皮膚病症諸如系 統性紅斑性狼瘡、系統性皮肌炎、乾癬;發炎性腸病、發炎 性眼病自體免疫性血液病及多發性硬化症的急性惡化;腎、 肝、心及其它器官移植;貝歇特氏(Behcet’s)急性視覺症候 群、内因性葡萄膜炎、過敏性皮炎、發炎性腸病、及腎病症 候群’何杰金氏病及非何杰金氏淋巴瘤、多發性肌瘤及慢性 淋巴細胞性白血病(CLL);自體免疫溶血性貧血及與Cll相 連結的血小板減少症;白血病及惡性淋巴瘤。 較佳可投予本發明化合物用於呼吸疾病例如從輕度至急 10Π08588 95 201247697 性重度氣喘及COPD病況的預防及/或治療。 現在將藉下列非限制性實施例進一步描述本發明。 於報告之實驗程序中,可使用下列縮寫:TEA==三乙基 胺,DCM=二氣曱烷;rt=室溫;Ac〇Et=乙酸乙酯;dmF —N,N-一曱基甲酼胺;DMSO=二曱亞石風;HATU= 〇-(7_σ丫 笨并一唾-1-基)-Ν,Ν,Ν’,Ν’-四曱基六氟鱗酸脲鏽。 [實施例1]
乙酸(8S,9S,10R,13S,14S,17R)-17-(2-乙醯氧基-乙醯 基)-10,13-二曱基_3,U_二側氧基 _6,7,8,9,10,11,12,13,14,15,16,17-十二氫_311_環戊|>]菲-17-基 酯(中間產物2)之製備 於乙酸2-((l〇R,13S,17R)-17-羥基-l〇,13_二曱基_3,U-二側 氧基-6,7,8,9,10,11,12,13,14,15,16,17-十二氫_311-環戊|>]菲 -17-基)-2-側氧基-乙基醋(中間產物1)(2克,4.99毫莫耳)及對 曱笨磺酸(PTSA)(200毫克,1.051毫莫耳)於乙酸(5毫升)之懸 浮液内於0°C以10分鐘時間徐緩添加三氟乙肝(5毫升,35.4 毫莫耳)。於0°C攪拌分鐘後,反應混合物於室溫攪拌3小 時。 反應混合物倒入冰/水(130毫升)内及所得混合物以 101108588 96 201247697 (2x100毫升)及乙酸乙酯(2xl〇〇毫升)萃版。 紱合有機萃取物 以無水硫酸納脫水及》農縮。粗產物於一帛仍 、一軋化矽凝膠上以從 匪至簡Ae0Et㈣之梯度洗提藉急迷層析術純化獲 得標題化合物(2.64克,定量產率)。 LC-MS (ESI POS): 445.2 (MH+) 乙酸(WsjoR’mwmHw·乙醯氧基乙醢 基)-11-經基-l〇,13-二甲基·3侧氧基 -6^9J0J142,13J4J5,16,17-+^A.3H.itA[a]W.17^ 酯(中間產物3)之製備 於中間產物2 (2.64克,5.97毫莫耳)於THF 〇5毫升)及甲醇 (15.00毫升)之冰冷溶液内’以2.5小時時間分成數份添加硼 虱化納(221毫克’ 5.84毫莫耳)。反應’/昆合物倒入1 n鹽酸及 冰(150毫升)内。形成的沈澱以乙酸乙酯(3xl〇〇毫升)萃取及 組合有機層以無水硫酸納脫水及濃縮。粗產物以Dcm至 DCM/AcOEt 40:60之梯度洗提於二氧化矽凝膠上藉急速層 析術純化獲得標題化合物(1.21克,45.6%產率)。 'H NMR (300 MHz, CHLOROFORM-d) ppm 7.28 (d, i h), 6.30 (dd, 1 H),6.05 (t,1 H),4.92 (d,1 H>,4.69 (d,1 H),4.48 - 4.58 (m,】H),2 75 · 2 91 (m,1 H), 2.61 (m,1 H),2.Π (ddd,1 H>,2.18 - 2.21 (m,3 H>,2 〇9 _ 2 28 (m,3 H),2.07 (s,3 H),1.74 - 1_98 (m,3 H),1.51 - l‘7〇 (m,! H),i 48 (s,3 H),1.26 · 1.39 (m,2 Η), l.ll - 1.19 (m,1 H),1.05 (s,3 H) LC-MS (ESI POS): 445.2 (MH+) [實施例2] 101108588 97 201247697
乙酸 2-((6S,8S,9R,10S,llS,13S,14S)_6,9_ 二氟七羥基 -10,13-二曱基-3-側氧基-^^儿⑴^^十二氫 -3H-環戊[a]菲-17-基)-2-側氧基_乙基酯(中間產物5)之製備 於丁酉夂(9尺,1〇8,118,138,17尺)-17-(2-乙醜氧基_乙醯基)_9_ 氯-11-經基-10,13-二曱基_3_側氧基 -6,7,8,9,10,11,12,13,14,15,16,17-十二氫-犯-環戊[&]菲-17-基 酯(中間產物4)(2.48克,4.88毫莫耳)於無水DMF (60毫升)之 溶液内於氮氣環境下添加乙酸鉀(3.83克,39.0毫莫耳)及反 應混合物於100°C攪拌1.5小時。冷卻後之反應混合物倒入冰 及鹽水(200毫升)内,水層以乙酸乙酯(3x150毫升)萃取。纽 合有機萃取物以水及食鹽水洗滌,以硫酸鈉脫水及濃縮獲得 2.55克粗產物標題化合物,其未經進一步純化即用於次一步 驟。 *H NMR (300 MHz, DMSO-i/6): ppm 7.29 (dd, 1 H), 6.99 (dd, 1 H), 6.29 (dd, 1 H), 5.98 - 6.15 (m, 1 H), 5.68 (dddd, 1 H), 5.56 (dd, 1 H), 5.l〇 (d, 1 H), 4.92 (d, 1 H), 3.98 - 4.23 (m, 1 H), 2.56 - 2.83 (m, 1 H), 2.26 - 2.44 (m,3 H), 2.14 - 2.26 (m, 1 H),2.09 (s,3 H>,1.7 卜 1.87 (m, 1 H)’ 1.55 · 1.65 (m,2H),1.53(s,3H),U5(s,3H). LC-MS (ESI POS): 421.97 (MH+) (68,88,9艮108,118,138,148)-6,9-二氟-1卜羥基-17-(2-羥基 101108588 98 201247697 -乙醯基)-10,13-二曱基_6,7,8,9,10,11,12,13,14,15-十二氫-環 戊[a]菲-3-酮(中間產物6)之製備 於(中間產物5)(2.55克,6.06毫莫耳)於乙醇(1〇〇毫升)之溶 ·: 液内,添加南極念珠菌脂解酶(2單位/毫克)(5i〇毫克,6.06 、 毫莫耳)及反應混合物於37°C攪拌隔夜。反應混合物經過 濾,以曱醇洗滌’及殘餘物以DCM/AcOEt 90:10至 DCM/AcOEt 50:50之梯度洗提’於二氧化石夕凝膠上藉急速層 析術純化獲得1.62克標題化合物(70.6%產率)。 'H NMR (3〇〇 MHz, DMSO-4): ppm 7.29 (dd, 1 H), 6.87 (dd, 1 H), 6.29 (dd, 1 H), 6.09 - 6.17 (m, 1 H), 5.67 (dddd, 1 H)s 5.53 (dd, 1 H), 4.77 (t, 1 H), 4.44 (dd5 1 H), 4.26 (dd, 1 H), 4.04 - 4.15 (m, 1 H), 2.56 - 2.79 (m, 1 H), 2.39 (dd, 1 H), 2.25 - 2.35 (m, 2 H), 2.09 - 2.25 (ra, 1 H), 1.76 (td, 1 H), 1.55 - 1.66 (m, 2 H), 1.53 (s, 3 H), 1.17 (s, 3 H). LC-MS (ESI POS): 379.99 (MH+) 表1列舉之中間產物7及8係始於中間產物3,如先前對中間 產物5及6所述製備。 [表1] 101108588 99 201247697 中間產物 結構式 產率 分析 7 50% LC-MS (ESI POS): 385.45 (MH+) *HNMR(300MHz, 氣仿-d ) ppm 7.32 (d, 1 H), 6.74 (dd, 1 H), 6.29 (dd, 1 H), 6.03 (t, 1 H), 5.02 (d, 1 H), 4.88 (d, 1 H), 4.36 - 4.51 (m, 1 H), 2.55 - 2.73 (m, 1 H), 2.21 - 2.54 (m, 5 H), 2.19 (s, 3 H), 2.05 - 2.18 (m, 1 H), 1.66 (dd, 1 H), 1.51 (s, 3 H), 1.28 (s, 3 H), 1.04 -1.44 (m, 4 H) 8 94% LC-MS (ESI POS): 343.2 (MH+) lH NMR (300 MHz, DMSO-d6) ppm 7.34 (d, 1 H), 6.83 (dd, 1 H), 6.16 (dd, 1 H), 5.92 (t, 1 H), 4.80 (d, 1 H), 4.74 (t, 1 H), 4.42 (dd, 1 H), 4.23 (dd, 1 H), 4.15 - 4.23 (m, 1 H), 2.53 -2.67 (m, 1 H), 2.43 (dd, 1 H), 1.94 -2.39 (m, 5 H), 1.42 - 1.48 (m, 1 H), 1.39 (dd,lH), 1.17(s,3H), 0.74-1.33 (m, 5 H) [實施例3]
(68,83,911,103,113,133,148)-17-(2-(第三丁基二曱基矽烷 基氧基)乙醯基)-6,9-二氟-11-經基-i〇,i3-二曱基 -6,7,8’9,10,11,12,13,14,15-十二氫-311-環戊[&]菲-3_酮(中間 產物9)之製備 於中間產物6 (300毫克,0.793毫莫耳)於無水DMF(12毫升) 之溶液内,添加咪唑(135毫克,1 982毫莫耳)及吡啶(〇321 毫升’ 3.96毫莫耳)’接著添加第三丁基氣二甲基魏(263 101108588 100 201247697 毫克,1.744毫莫耳)。反應於室溫攪拌2小時。完成轉換。 反應以乙酸乙酯稀釋及以水洗條’水層以乙酸乙酯萃取兩 次及然後組合萃取物以硫酸鈉脫水及蒸發。粗產物於二氧化 矽凝膠(DCM,DCM/AcOEt 8:1)上透過層析術管柱純化獲得 365毫克(93%產率)。 LC-MS (ESI POS): 493.1 (MH+) [實施例4]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-jLf*_ 丁基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 _4&’415’5,6,6&,613,8,9,9&,10,1〇3,101),11,12-十四氫-7-呤-8-口丫- 戊搭烯并[2,l-a]菲_2-酮(化合物1〇)之製備 中間產物6(1.3克,3.44毫莫耳),N-(3,3-二曱基丁基)羥基 胺(826亳克’ 7.〇5毫莫耳)及三聚曱醛(0.650克,21.64毫莫耳) 於乙醇(50毫升)之混合物回流攪拌隔夜。蒸發去除溶劑及粗 產物藉二氧化矽凝膠層析術純化〇DCM/MeOH 98:2)獲得化 合物9 (1.56克,3.07毫莫耳,89%產率)。 101108588 101 201247697 'H NMR (300 MHz, DMSO-d6) ppm 7.25 (dd, 1 H) 6.29 (dd, 1 H) 6.1 L (s, 1 H) 5.49 - 5.79 (m, 1 H) 5.44 (d, 1 H) 4.77 (t, 1 H) 4.48 (dd, 1 H) 4.12 - 4.24 (m, 1 H) 4.12 (dd, 1 H) 3.43 - 3.60 (m, 1 H) 3.31 - 3.43 (m, 1 H) 2.54 - 2.72 (m, 3 H) 2.08 - 2.34 (m, 2 H) 1.80 - 2.01 (m, 2 H) 1.51 - 1.71 (m, 3 H) 1.49 (s, 3 H) 1.18 -1.46 (m, 3 H) 0.86 (s, 9 H) 0.81 (s, 3 H) LC-MS (ESI POS): 508.26 MH+ [ah25 = + 131.4 (c 0.213; CHC13) 表2列舉之化合物係如前文對化合物10所述藉中間產物 6、8或9與適當羥基胺或羥基胺鹽酸鹽之環化加成製備。 終化合物係藉二氧化矽凝膠管柱層析術或製備性HPLC純 化。 [表2]
結構式_
產率 88% _合析_ LC-MS (ESI P0S): 532.03 (MH+) [α]〇25 = +175.3 (c=0.22, CHCb) *H NMR (300 MHz, DMSO-di) ppm 7.28 - 7.37 (m, 2 H), 7.26 (dd, 1 H), 7.01 - 7.18 (m, 2 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.50 - 5.78 (m, 1 H), 5.43 (dd, 1 H), 4.57 - 4.77 (m, 1 H), 3.99 - 4.26 (m, 2 H), 3.89 (d, 1 H), 3.83 - 3.95 (m, 1 H), 3.75 (d, 1 H), 3.43 - 3.60 (m, 1 H), 3.34 - 3.43 (m, 1 H), 2.57 - 2.69 (m, 1 H), 2.04 -2.36 (m, 3 H), 1.78 - 1.99 (m, 1 H), 1.52 - 1.72 (in, 3 H), 1.49 (s,3 H), 1.38- 1.48 (m, 1 H),0.80 (s,3 H)_ 101108588 102 201247697 12 ^:Γ0 F 43% LC-MS (ESI POS): 519.98 (MH+) [a]DZ5 = + 129.9° (c = 0.63, CHC13) iHNMRpOOMHADMSO· de) ppm 7.40 - 7.47 (m, 1 H), 7.26(dd,lH), 6.83 -7.03 (m, 2 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.49-5.80 (m,lH), 5.45 (dd, 1 H), 4.72 (br. s., 1 H), 4.33 (dd, 1 H), 4.09 - 4.24 (m, 2 H), 3.88-4.07 (m, 2 H), 3.43 -3.60(m, 1H), 3.34-3.43 (m, 1H), 2.55 - 2.70 (m, 1H), 2.04 -2.39 (m, 3 H), 1.90 - 2.03 (m, 1H), 1.51-1.71 (m, 3 H), 1.49 (s,3H),1.37-1.47(m,lH), 0.81 Cs,3H) JH 〇 LC-MS (ESI POS): 504.02 (MH+) [a]〇2S = + 133.1° (c = 0.30, CHC13) 'H NMR (300 MHz, DMSO-d^) ppm 7.55 (dd, 1 H), 7.26 59% (dd, 1 H), 6.40 (dd, 1 H), 6.22 13 F -6.35 (m, 2 H), 6.12 (s, 1 H), 5.49 - 5.78 (ra, 1 H), 5.43 (d, 1 H), 4.71(3 br, 1H), 4.27 (d, 1 H), 3.99 (d, 1 H), 3.92 (d, 1 H), 3.82 (d, 1 H), 3.35 - 3.54 (m, 3 H), 2.55 - 2.71 (m, 1 H), 2.01 - 2.31 (m, 3 H), 1.84 -1.98 (m, 1 H), 1.51 -1.68 (m, 3 H), 1.49 (s, 3 H), 1.42 (dd, 1 H), 0.81 (s,3H) 103 101108588 201247697 14 10% LC-MS (ESI POS): 508.45 MH+ [a]D25 = + 126.4 (c 0.135, CHCls) *H NMR (300 MHz, DMSO-d6) ppm 7.25 (dd, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.49- 5.81 (m, 1 H), 5.44 (dd, 1 H), 4.81 (ts 1 H), 4.45 (dd, 1 H), 4.15 - 4.24 (m, 1 H), 4.12 (dd, 1 H), 3.42 - 3.60 (m, 1 H), 3.33 - 3.43 (m, 1 H), 2.55 -2.70 (m, 1 H), 2.06 - 2.34 (m, 2 H), 1.83 - 2.06 (m, 2 H), 1.50-1.71 (αι,3Η), 1.49 (s, 3 H), 1.12 - 1.46 (m, 8 H), 0.62 -0.92 (m, 9 H) 15 P 41% LC-MS (ESI POS): 572.42 MH+ [a]D25 = + 148.3 (c 0.2 MeOH) *H NMR (300 MHz, DMSO-d6) ppm 7.90 (s, 1 H), 7.87 (dt, 1 H), 7.55 (dt, 1 H), 7.47 (t, 1 H), 7.26 (dd, 1 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.48 -5.81 (m, 1 H), 5.43 (dd, 1 H), 4.67 (br. s., 1 H), 3.84 - 4.26 (m, 5 H), 3.83 (s, 3 H), 3.45 -3.60 (m, 1 H), 3.34 - 3.45 (m, 1 H), 2.56 - 2.71 (m, 1 H), 2.05 - 2.36 (m, 3 H), 1.81 -1.97 (m, 1 H), 1.51 - 1.70 (m, 3 H), 1.49 (s, 3 H), 1.36-1.46 (m, 1 H), 0.80 (s, 3 H) 104 101108588 201247697 16 71% LC-MS (ESI POS): 520.45 MH+ [a]D25 = + 150.2 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-d«) ppm 7.25 (dd, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.49-5.82 (m, 1 H), 5.44 (dd, 1 H), 4.80 (t, I H), 4.45 (dd, 1 H), 4.16-4.25 (m,lH), 4.12 (dd, 1 H), 3.40 - 3.56 (m, 1 H), 3.32 - 3.40 (m, 1 H), 2.56 -2.71 (m, 1 H), 2.05 - 2.33 (m, 2 H), 1.85 - 2.05 (m, 2 H), 1.75 (dd, 1 H), 1.51 - 1.70 (ra, 7 H), 1.49 (s, 3 H), 1.41 (dd, 1 H), 1.03 - 1.31 (m, 5 H), 0.83 - 1.00 (m, 3 H), 0.81 (s, 3H) 17 β 70% LC-MS (ESI POS): 560.3 MH+ [a]D25 = + 203.5 (c 0.2 MeOH) *H NMR (300 MHz, DMSO-d«) ppm 7.07 - 7.36 (m, 5 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.48 - 5.77 (m, 1 H), 5.43 (d, 1 H), 4.48 - 4.82 (m, 1 H), 4.02 - 4.29 (m, 2 H), 3.87 -3.98 (m, 1 H), 3.86 (d, 1 H), 3.73 (d, 1 H), 3.32 - 3.54 (m, 2 H), 2.55 - 2.67 (m, 1 H), 2.45 (s, 3 H), 2.01 - 2.31 (m, 3 H), 1.91 (d, 1 H), 1.48 (s, 3 H), 1.33 - 1.73 (m, 4 H), 0.80 (s,3H) 105 101108588 201247697 18 23% LC-MS (ESI POS): 480.34 MH+ [α]〇2ί = + 84.1 (c 0.2 MeOH) lH NMR (300 MHz, DMSO-d«) ppm 7.25 (dd, 1 H), 6.29 (dd, 1 H), 6.04 - 6.19 (m, 1 H), 5.49 - 5.77 (m, 1 H), 5.37 -5.49 (m, 1 H), 4.47 (d, 1 H), 4.16 - 4.21 (m, 1 H), 4.12 (d, 1 H), 3.25 - 3.42 (m, 2 H), 2.57 - 2.68 (m, 1 H), 1.87 -2.25 (m, 4 H), 1.50 - 1.69 (m, 3H), 1.49 (s, 3 H), 1.22-1.47 (m,4 H), 0.90 及 1.05 (d,3 H), 0.76 - 0.87 (m, 6 H) 19 0^:Γθ 82% LC-MS (ESI POS): 506.25 MH+ [a]D25 = + 151.5 (c 0.2 MeOH) lU NMR (300 MHz, DMSO-ϋβ) ppm 7.25 (dd, 1 H), 6.29 (dd,lH), 6.11(s, 1H), 5.48-5.75 (m, 1 H), 5.38 - 5.46 (m, 1 H),4.71 - 4.86 (m, 1 H), 4.48 (dd, 1 H), 4.15 - 4.23 (m, 1 H), 4.11 (dd, 1 H), 3.42 -3.58 (m, 1 H), 3.32 - 3.42 (m, 1 H), 2.57 (d, 2 H), 2.35 - 2.45 (m, 1 H), 1.86 - 2.19 (m, 6 H), 1.51 - 1.78 (m, 6 H), 1.49 (s, 3 H), 1.34 - 1.45 (m, 2 H), 1.03 -1.22 (m, 3 H), 0.82 (s, 3 H) 106 101108588 201247697 20 39% LC-MS (ESI POS): 614.29 MH+ [a]D25 = + 208.5 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.76 -7.90 (m, 2 H), 7.32 -7.48 (m, 2 H), 7.25 (dd, 1 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.48 -5.82 (m, 1 H), 5.42 (dd, 1 H), 4.63 - 4.77 (m, 1 H), 4.10 - 4.22 (m, 1 H), 3.71 - 4.10 (m, 4 H), 3.46 - 3.62 (m, 1 H), 3.35 - 3.46 (m, 1 H), 2.57 - 2.70 (m, 1 H), 2.06 - 2.36 (m, 2 H), 1.79 - 1.96 (m, 1 H), 1.57 - 1.67 (m, 4 H), 1.54 (s, 9 H), 1.49 (s,3H), 1.36-1.51 (m, lH),0.80(s,3H) 21 Γ 84% LC-MS (ESI POS): 547.99 (MH+) !H NMR (300 MHz, DMSO-cfe) ppm 7.20 -7.43 (m, 5 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.50 -5.81 (m, 1 H), 5.43 (dd, 1 H), 4.54 - 4.78 (m, 1 H), 4.00 - 4.23 (m, 2 H), 3.81 - 3.97 (m, 2 H), 3.74 (d, 1 H), 3.33 - 3.59 (m, 2 H), 2.55 - 2.63 (m, 1 H), 2.01 - 2.35 (m, 3 H), 1.77 - 1.96 (m, 1 H), 1.51 - 1.69 (m, 3 H), 1.49 (s, 3 H), 1.35-1.46 (m, 1H), 0.80 (s, 3 H) 107 101108588 201247697 22 P 86% LC-MS (ESI POS): 644.0 (MH+) 23 OH J J:7 P 40% LC-MS (ESI POS): 522.13 MH+ Md25 = + 133.6 (c 0.2 MeOH) 'HNlV[R(300MHz, DMSO-de) ppm 7.26 (dd, 1 H), 6.29 (dd, 1 H), 6.07 -6.17 (m, 1 H), 5.48-5.79 (m, 1 H), 5.43 (dd, 1 H), 4.79 (t, 1 H),4.44 (dd,lH), 4.16-4.22 (m, 1 H),4.12 (dd, 1 H), 3.31 - 3.49 (m, 2 H), 2.55 - 2.66 (m, 1 H), 2.41-2.47(m,lH),l_83-2.32(m,5H), 1.50- 1.70 (m,3H),1.49 (s,3H), 1.11 -1.46 (m, 8 H), 0.85 (t, 6 H), 0.81 (s, 3 H) 24 β 68% LC-MS (ESIPOS): 570.18 MH+ [a]D25 = +122.4 (C 0.149, CHC13) 'H NMR (300 MHz, DMSO-d6) ppm 7.28-7.34 (m, 2 H), 7.26 (dd, 1 H), 7.15 - 7.22 (m,2H)>6.30(ddf 1H), 6.11 (s, 1 H), 5.48 - 5.79 (m, 1 H), 5.43(dd, 1H), 4.57-4.82 (ra,lH),4.29(dd, 1H),4.I1 -4.22(m, lH),3.98(dd,l H), 3.87 (d, 1 H), 3.79 (d, 1 H),3.31-3_51(m,2H),2.55 -2.68 2.01-2.32 H), 1.51-1.74(10,2 H), 1.48 (s, 3 H), I.29-1.44(m,2H), 1.25 fs, 9 H), 0.80 Cs,3H) 108 101108588 201247697
101108588 109 71% LC-MS (ESIPOS): 556.25 MH+ [0^ = +151.3(0 0.147, CHC13) 'HNMR(300 MHz, DMSO-de) ppm 7.26 (dd, 1H), 7.14 - 7.20 (m, 2 H), 7.06 - 7.14 (m, 2 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.49 - 5.77 (m, 1 H), 5.43 (dd, 1 H), 4.66 (br. s., 1 H), 4.08-4.31 (m,2H), 3.92 (d, 1 H), 3.85 (d, 1 H), 3.76 (d, 1 H), 3.33 -3.51 (m, 2 H), 2.58-2.71 (m, 1 H), 2.44 - 2.48 (m, 2 H), 1.99 - 2.33 (m, 3 H), 1.80 - 1.98 (m,lH), 1.50 -1.70 (ra, 5 H), 1.47 (s, 3 H), 1.31 -1.45 (m, 1 H), 0.87 (t, 3 H), 0.80 (s, 3 H) 69% LC-MS (ESI POS): 506.29 MH+ [a]〇25 = + 97.8 (c0.2 MeOH) 1HNMR(300MHz, DMSO-d<) ppm 7.25 (dd, 1H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.49 - 5.74 (m, 1 H), 5.43 (dd, 1 H), 4.76 (t, 1 H), 4.49 (dd, 1 H), 4.13 -4.22 (m, 1 H), 4.12 (dd, 1 H), 3.41 - 3.61 (m, 1 H), 3.31-3.41 (m,lH), 2.54 -2.69 (m,lH), 2.31 -2.44(m,lH), 1.82-2.31 (m,5H),1.50-1.76(ra,6 H), 1.49 (s, 3 H), 1.35 -1.46 (m,1 Η), 0.97 -1.30 Cm, 6 H), 0.81 (s, 3 H) 201247697 10Π08588 27 F 77% LC-MS (ESI POS): 494.17MH+ [«]d2S = +242.2 (c 0.09, CHC13) 'HNMRiSOOMHz, DMSO-de) ppm 7.25 (dd, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H)s 5.48 - 5.80 (m, 1 H), 5.44 (d, 1 H), 4.78 (dd, 1H), 4.47 (dd,lH), 4.11-4.22 (m, 1 H), 4.12 (dd, 1 H), 3.41 -3.58 (m, 1 H), 3.32 - 3.42 (m, 1 H), 2.55 -2.71 (tn, 3 H), 2.03 -2.37 (m, 2 H), 1.83-2.03 (m,2H), 1.50- 1.72 (m, 4 H), 1.49(5,3¾ 1.27-1.46 (m, 3 H), 0.85 (d, 3 H), 0.85 (d, 3 H), 0.81 (s, 3H) OH 66% LC-MS (ESI POS): 566.13MH+ [a]D25 = + 140.2 (c 0.119, CHCI3) hnmrcsoomhz, DMSO-de) ppm 7.26 (dd, 1 H), 6.95 (d, 1 H), 6.85 (d, 1 H), 6.30 (dd, 1 H), 28 6.11 (s,lH), 5.48-5.79 F (m, 1 H), 5.44 (dd, 1 H), 4.38 (d, 1H), 4.08-4.25 (m, 2 H), 4.03 (d, 1 H), 3.95 (d, 1 H), 3.38-3.51 (m, 2 H), 2.56 - 2.68 (m, 1 H), 2.41 (s, 3 H), 2.03 -2.32 (m, 3 H), 1.89-2.04 (m,lH),l_51-1.71(m,4 H), 1.49 (s, 3 H), 1.34-1.45 (m, 1 H), 0.81 (s, 3 H) 110 201247697 29 β 58% LC-MS (ESI POS): 508.22 MH+ [a]D25 = +118.8 (c 0.26, MeOH) lHNMR(300 MHz, DMSO-d6) ppm 7.25 (d, 1 H), 6.29(dd, 1H), 6.11 (s, 1 H), 5.46-5.81 (m,lH), 5.43 (d, 1 H), 4.81 及 4.83 (t, 1 H), 4.48 (dd, 1 H), 4.13-4.25 (m,lH), 4.10 及 4.13 (dd, 1 H), 3.31-3.53(m,2H),2.53-2.70 (m, 2 H), 2.27 (dt, 2 H), 2.02 - 2.21 (m, 3 H), 1.87-2.01(m,lH),1.68-1.87 (m,lH), 1.53 (s,3 H), 1.36- 1.68 (m, 4 H), 0.88 及 0.95 (t, 3 H), 0.84 及 0.85 (d, 3 H), 0.82 (s, 3 H), 0.75 及 0_82 (d, 3 H) 30 F 69% LC-MS (ESI POS): 596.09 MH+ Wd25 =+ 154.9 (c 0.2 MeOH) 'HNMR(300 MHz, DMSO-d6)ppm 7.26 (dd, 1 H), 7.16 (m, 2 H), 6.84 (m, 2 H), 6.30 (dd, 1 H), 6.12 (s,lH), 5.47-5.79 (m, 1 H), 5.42 (d, 1 H), 4.50 - 4.77 (tn, l H), 4.05 -4.26 (m, 2 H), 3.94 (m, 3 H), 3.59 - 3.86 (m, 2 H), 3.33 - 3.46 (m, 1 H), 1.98-2.31 (m,3H), 1.93 (d, 1 H), 1.51-1.79 (m, 5 H), 1.49 (s, 3 H), 1.36-1.47 (m, 3 H), 0.93 (t, 3 H), 0.80 (s, 3 H) 111 101108588 201247697 101108588 31 32
112 65% 8% LC-MS (ESI POS): 534.28 MH+ [a]〇25-+152.3 (c 0.23, MeOH) *HNMR(300 MHz, DMSO-d6) ppm 7.25 (dd, 1H), 6.29(dd, 1H), 6.11 (s,1 H),5.48 · 5.78 (m, 1 H), 5.44 (dd,lH), 4.78 (t· 1 H), 4.46 (dd, 1 H), 4.12 -4.24 (m, 1 H), 4.12 (dd.1 H)F 3.42-3.57 (mflH), 3.31-3.41 2.56- 2.74 (m, 3 H), 2.02-233 (m, 2 H), 1.83- 1.97 (m, 2 H), 1.51-1.72 (m, 8 H), 1.49 (s, 3 H), 1:04-L46 (m, 7 H), 0.83 - 0.97 (ms 2 H), 0.81 (s, 3 H)_ LC-MS (ESI POS): 567.23 M+ [a]D25 = +110(c0.26, MeOH). 'HNMR(300 MHz, DMSO-dfi) ppm 7.55 (d, 1 H), 7.38 (d, 1 H), 7.28 (dd, 1 H), 7.22 (s, 1 H), 7.13 (ddd, 1 H), 7.00 (ddd, 1 H), 6.32 (dd, 1H), 6.14(s, 1 H), 5.49-5.81 (mJH), 5.45 (dd, 1H), 4.65 (br.s., 1 H), 3.83 - 4.38 (m, 5 H), 3.72 (s, 3 H), 3.30-3.49 (m, 2 H), 2.55 - 2.69 (m, 1 H), 1.95-2.36 (m, 4 H), 1.52 - 1.71 (m, 3 H), 1.50 (s, 3 H), 1.41 (dd, 1 H), 0.82 (s, 3 H) _ 201247697 LC-MS (ESI POS): 518.11 MH+ [cx]D25 = + 108.5 (c 0.24, MeOH) ·_ OH iHNMRGOOMHz, DMSO-di) ppm 7.25 (d, 1 H), 6.29 (dt,lH), 6.11(s, 33 80% 1 H), 5.48 -5.86 (ιη,ΙΗ), 5.43 (d, 1 H),4_76 及 4.83 (t, 1 H), 4.30 - 4.67 Γ T fTr (m, 1 H), 4.05 - 4.24 (m31 H), 4.08 (dd,lH), 3.35- 3.60 (m, 2 H),2.55-2/75 (m,2H)s 2,18-2.37^1 H),2.10(br. s.,2H),1.81 -2.05 (m, 2 H), 1.32-1.68 (m,5H), 1.48 (s^H), 1.12 -1.32 (m, 4 H), 0.93-1.12(m,3H),0.79 及 0.82 (s, 3 H), 0.58 - 0.90 及 0.84 -0.96 LC-MS (ESI POS): 543.24 MH+ [cc]D25 = + 136.9 (c 0.3, MeOH) 4 NMR (300 MHz, DMSO-de) ppm 8.33 - OH 8.48 (ra, 2 H), 7.60 (dt, 1 34% H), 7.29 (ddd, 1 H), 7.25 (dd, 1 H), 6.29 (dd, 1 H), 34 6.11 (s, 1 H), 5.49 - 5.80 (m, 1 H), 5.44 (dd, 1 H), 4.83 (t, 1 H), 4.51 (dd, 1 •· H), 4.14-4.23 (m,lH), 4.13 (dd,lH)? 3.44-3.57 (m, 1 H), 3.33 - 3.44 (m, 1 11),2.57-2.81(111,5¾ 2.06-2.33(ra,2H),1.86-2·03(ιη,2Η),1.69·1.85 (m,2H),1.51 - 1·69(ηι,3 H), 1.49 (s, 3 H), 1.42 (dd, 1 H), 0.82 (s, 3 H) 113 101108588 201247697 35 16% LC-MS (ESI POS): 520.17 MH+ [α]〇25 = + 123.8 (c 0.27, MeOH) 'HNMR(300 MHz, DMSO-de) ppm 7.25 (dd, 1H), 6.29(dd, 1H), 6.11 (s, 1 H), 5.50 - 5.80 (m, 1 H), 5.45 (dd, 1 H), 4.81 (t, lHX4.43(dd,lH),4.14-4.24 (m, 1 H), 4.14 (dd, 1 H), 3.47 - 3.64 (m, 1 H), 3.33 - 3.47 (m, 1 H), 2.89 -3.10(ra, 1H), 2.76-2.89 (m, 1 H), 2.58 - 2.70 (m, 2 H), 2.38 - 2.46 (m, 1 H), 1.85 - 2.35 (m, 4 H), 1.53-1.72 (m, 3 H), 1.49 (s, 3 H), 1.43 (dd, 1 H), 0.82 (s, 3H) 36 #〜0 F 62% LC-MS (ESI POS): 518.25 MH+ [<x]D25 = + 122.2 (c 0.1435; MeOH) ^NMRCSOOMHz, DMSO-de) ppm 7.57 (s, 1 H), 7.26 (dd, 1 H), 7.12 (t, 1 H), 6.83 (s, 1 H), 6.30 (dd, 1 H), 6.12 (s, 1 H)} 5.50 - 5.83 (m, 1 H), 5.45 (dd, 1 H), 4.86 (t, 1 H), 4.45 (dd, 1 H), 4.01 - 4.24 (m, 4 H), 3.35-3.51 (m,2 H), 3.03 - 3.21 (m, 1 H), 2.87 - 3.03 (m, 1 H), 2.58 -2.71 (m, 1 H), 1.86-2.30 (m,4H), 1.52- 1.76 (m, 3 H), 1.49 (s, 3 H), 1.42 (dd, 1 H), 0.82 (s, 3 H) 114 101108588 201247697 37 18% LC-MS (ESI POS): 565.27 MH+ [a]D25 = + 193.2 (c 0.25, MeOH) 'HNMR(300MH2, DMSO-d^) ppm 8.89 (dd, 1 H), 8.55 (dt, 1 H), 7.97 (d,lH), 7.70(dd,lH), 7.54 (dd, 1 H), 7.49 (dd, 1 H), 7.27 (dd, 1 H), 6.32 (dd, 1 H), 6.14 (s, 1 H), 5.49 - 5.80 (m, 1 H), 5.42 (dd, 1 H), 4.53 (br. s., 1 H), 4.38 (d, 1 H), 4.29 (d, 1 H), 4.09 - 4.22 (m, 1 H), 3.66-3.91 (m, 2 H), 3.53 (br. s., 1 H), 3.37 (br. s., 1 H), 2.54 - 2.70 (m, 1 H), 2.15 - 2.35 (m, 3 H), 1.83 -1.97 (m,lH), 1.52-1.72 (m, 3 H), 1.49 (s, 3 H), 1.39 - 1.46 (m, I H), 0.78 (s,3H) 38 Ψ 29% LC-MS (ESI POS): 521.22 MH+ [a]D25 = + 172.7 (c 0.33, MeOH) lHNMR(300MHz, DMSO-de) ppm 7.73 (d, 1 H), 7.69 (d, 1 H), 7.26 (dd, 1 H), 6.30 (dd, 1 H), 6.12 (s,lH), 5.49-5.79 (m,l H), 5.44 (dd, 1 H), 4.81 (t, 1 H), 4.38 (dd,lH), 4.07-4.23 (m, 1 H), 4.06 - 4.39 (m, 2 H), 3.99 (dd, 1 H), 3.53 - 3.74 (m,lH), 3.41 - 3.53 (m,lH), 2.56-2.71 (m, 1 H), 2.07 - 2.36 (m, 3 H), 1.82- 1.97 (m,lH), 1.51 -1.69 (m, 3 H), 1.49 (s,3H), 1.38- 1.47 (m, 1 K), 0.81 (s, 3 H) 115 101108588 201247697 [實施例5]
曱烷磺酸2-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,43,413,5,6,68,8,9,9&,10,1(^,101),11,12-十四氫-7-»号-8-吖-戊 搭婦并[2,1-a]菲-6b-基]-2-側氧基-乙基g旨(化合物39)之製備 於化合物21 (200毫克,0.365毫莫耳)於無水°比咬(8毫升) 之溶液内於氮氣環境下添加曱烷磺醢氣(0.057毫升,0.730 毫莫耳)。攪拌3小時後,又添加曱烧續酿氯(0.057毫升,0.730 毫莫耳)。反應混合物又於室溫攪拌1小時。 反應混合物倒入2 Ν鹽酸(80毫升)及冰内,所形成之沈殿 經過濾及以冷1Ν鹽酸及水洗務;然後過遽出之固體溶解於 DCM。所得有機相以無水硫酸鈉脫水及漠縮獲得222毫克期 望化合物74 (97%產率)。 LC-MS (ESI POS): 626.3 (MH+) (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-乙醯基-8-(4- 氯-苄基)-4b,12-二氟-5-經基_4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+Es^_7_«m 戊搭烯并[2,l-a]菲-2-酮(化合物40)之製備 化合物39 (308亳克,0.492毫莫耳)溶解於丙酮(12毫升)及 101108S88 116 201247697 添加蛾化鈉(738毫克,4.92毫莫耳)。反應混合物於65〇c攪拌 隔夜。反應混合物以乙酸乙酯(80毫升)稀釋,以飽和硫代硫 酉文鈉洗條直到块消失,然後以飽和碳酸氫納洗條。有機層以 硫酸鈉脫水及蒸發’獲得224毫克粗產物,轉製備性HPLC 純化獲得65毫克純質化合物75 (25%產率)。 lH NMR (300 MHz, DMSO-d6) ppm 7.33 - 7.42 (m, 2 H), 7.28 - 7.33 (m, 2 H), 7.26 (d, 1 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.48 - 5.80 (m, 1 H), 5.43 (br. s., 1 H), 4.07 - 4.27 (m, 1 H), 3.93 (d, 1 H), 3.74 (d, 1 H), 3.44 - 3.57 (m, 1 H), 3.34 - 3.44 (m, 1 H), 2.56 - 2.76 (m, 1 H), 2.05 - 2.36 (m, 3 H), 1.91 -2.04 (m, 1 H), 1.88 (s, 3 H), 1.52 - 1.69 (m, 3 H), 1.49 (s, 3 H), 1.43 (dd, 1 H), 0.79 (s, 3 H) LC-MS (ESI POS): 532.28 (MH+) [a]D25 = + 285.8 (c 0.11, CHCij) [實施例6]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣苄 基)-4b,12-二氣-5-經基-4a,6a-二甲基-2-側氧基 •2,4\413,5,6,6\8,9,9110,10&,101),11,12-十四氫-7-吟-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸(化合物41)之製備 於化合物21(1.55克,2.83毫莫耳)於四氫呋喃(60毫升)及水 (30.0毫升)之溶液内於0°C逐滴添加6 N氫氧化鈉(1.414毫 升,8.49毫莫耳)及反應混合物於0°C攪拌10分鐘及於室溫攪 117 101108588 201247697 拌56小時。蒸發去除四氫呋喃,水層以pH 1酸化及以乙酸乙 醋(1〇〇毫升X3)萃取。組合有機萃取物以鹽水洗滌,脫水(硫 酸鈉)及濃縮。粗產物於DCM/AcOEt/HC02H 60:39.5:0.5藉二 氧化矽凝膠急速層析術純化獲得1.11克純質化合物(R P 〇. 3 4 於DCM/AcOEt/HC02H 50:49.5:0.5)。 LC-MS (ESI POS): 534.2 (MH+) 表3列舉之化合物係如先前對化合物41所述製備: [表3] 化合物 結搆式 產率 42 r 89% LC_MS (ESI POS): 494.2 (MH+) 43 62% LC_MS (ESI POS): 518.1 (MH+) 44 55% LC_MS (ESI POS): 506.1 (MH+) 45 F 41% LC MS (ESI POS): 490.1 (MH+) 46 20% LC MS (ESI POS): 52〇Tl (MH+) 47 F 99% LC MS (ESI POS): 53〇Tl (MH+) 101108588 118 201247697 48 96% LC MS (ESI POS): 480.1 (MH+) 49 71% LC MS (ESI POS): 492.1 (MH+) 50 43% LC MS (ESI POS): 542.1 (MH+) 51 98% LC MS (ESI POS): 514.1 (MH+) 52 97% LC MS (ESI POS): 540.0 (MH+) 53 i 97% LC MS (ESI POS): 514.2 (MH+) 54 P 50% LC MS (ESI POS): 556:2 (MH+) 55 F 59% LC MS (ESI POS): 546.1 (MH+) 56 F 78% LC MS (ESI POS): 508.1 (MH十) 119 101108588 201247697 57 99% LC MS (ESI POS): 530.1 (MH+) 58 P 31% LC MS (ESI POS): 524.0 (MH+) 59 P 63% LC MS (ESI POS): 492.1 (MH+) 60 68% LC MS (ESI POS): 494.1 (MH+) 61 j會 f 44% LC MS (ESI POS): 572.2 (MH+) 62 f 79% LC MS (ESI POS): 572.2 (MH+) 63 F 91% LC MS (ESI POS): 504.0 (MH+) 64 95% LC MS (ESI POS): 552.1 (MH+) 65 99% LC MS (ESI POS): 494.1 (MH+) 66 P 60% LC MS (ESI POS): 506.0 (MH+) 120 101108588 201247697 67 I Ρ 88% LC MS (ESI POS): 464Tl (ΜΗ+) 68 72% LC MS (ESI POS): 520:2 (MH+) 69 争 97% LC MS (ESI POS): 504.1 (MH+) 70 Ρ 96% LC MS (ESI POS): 553.2 (MH+) [實施例7]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-节 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-。号-8_。丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-(2-側氧基-[1,3]二哼嗦-4-基) 酯(化合物71)之製備 於化合物41(300毫克,〇.562毫莫耳)於無水DMF(11.2毫升) 之溶液内維持於氮氣下添加HATU (235毫克,0.618毫莫 耳)’接著添加N-曱基咮淋(0.062毫升,0·562毫莫耳)。反應 混合物於65¾加熱40分鐘’隨後轉換成活化酯完成。混合物 101108588 121 201247697 冷卻至室溫及分成數份添加NaSH(94毫克,丨685毫莫耳卜 溶液轉成深綠色於室溫攪拌20分鐘,然後逐滴添加馭氯-^ 二哼嗦-2-酮(206毫克,L685毫莫耳)’接著添加碘化鉀(46 6 毫克,0.281毫莫耳)’及混合物於室溫攪拌隔夜。添加乙酸 乙酯(70毫升)及混合物以鹽水洗滌;水層以乙酸乙酯(2χ7〇 毫升)萃取及組合有機萃取物以1 Ν鹽酸溶液及鹽水洗滌。有 機相以硫酸鈉脫水及蒸發,獲得940毫克粗產物,於 DCM/AcOEt 30:1至DCM/AcOEt 5:1之梯度洗提,透過層析 術管柱於二氧化矽凝膠上純化獲得32〇毫克期望化合物。進 一步透過製備性HPLC純化(動相:水/ACN不含酸性添加物) 獲得140毫克固體(39%產率)。^-NMR分析顯示存在有來自 於碳酸酯水解之盤。 'H NMR (300 MHz, DMSO-d6) ppm 7.18 - 7.42 (m, 5 Η), 6;26 - 6.38 (m, 2 H),6,13 (s,1 H),5.45 - 5.80 (m,2 H),4.88 及 4.92 (t, 1 H),4.33 及 4.42 (dd,1 H),4.09.4.24 (m,1 H), 3.99 及 4.02 (d,1 H),3.84 及 3.85 (d,1 H), 3.45 - 3.60 (m, 1 H), 3.34 - 3.45 (m, 1 H), 2.56 - 2.70 (m, 1 H), 1.97 - 2.34 (m, 4 H),1.52 - 1.91 (m,4 H),1.48 及 1.49 (s, 3 H),0.90 及.0.92 (s,3 H) LC-MS (ESI POS): 636.35 (MH+) [實施例8]
(4aS,4bR,5S,6aS,6bR,9aS, 1 OaS, 1 ObS, 12S)-8-(4-氯 _ 节 基)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基 10U08SS8 122 201247697 -2,4&,413,5,6,6&,8,9,9&,10,10&,101?,11,12,十四氫,7“号-8-。丫_戊搭 烯并[2,l-a]#_6b-羧酸甲氧基-甲基-醯胺(化合物72)之製備 於化合物41 (3Ό0毫克,0.562毫莫耳)於無水DMF (1〇.6毫 升)之溶液内,維持於氮氣環境下,添加HATU (235毫克, 〇.618毫莫耳)接著添加N-曱基咮啉(〇·〇62毫升,0.562毫莫 耳)。混合物於70°C攪拌40分鐘,隨後完成轉化成活化酯。 反應冷卻至室溫及添加N,〇-二曱基羥基胺鹽酸鹽(164毫 克,1.685毫莫耳)’接著添加TEA(〇 313毫升,2 247毫莫耳)。 /tb合物於室溫搜拌隔夜。進一步完成n,〇_二甲基經基胺鹽酸 鹽(164毫克’ 1.685毫莫耳),及TEA (0.313毫升,2.247毫莫 耳)之添加,及混合物於65〇c攪拌5小時。完成轉化。混合物 以乙酸乙酯(60毫升)稀釋及以鹽水(60毫升)洗滌。水層以乙 酸乙酯(2x60毫升)萃取,及然後有機萃取物以! >^鹽酸溶液 洗滌,以硫酸鈉脫水及蒸發。粗產物(7〇〇毫克)透過製備性 HPLC純化(中性動相),獲得96毫克純質固體(30%產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.27 - 7.39 (m, 4 Η), 7.24 (dd, 1 Η), 6.29 (dd, 1 Η), 6.12 (s, 1 Η), 5.46 - 5.75 (m, 1 Η), 5.36 (d, 1 Η), 4.02 -4.21 (m, 1 Η), 3.72 - 3.97 (m, 3 Η), 3.38 - 3.63 (m, 1 Η), 3.29 (s, 3 Η), 2.98 (br. s., 3 Η), 2.56 - 2.66 (m, I H), 2.03 - 2.34 (m, 3 H), 1.69 - 2.01 (m, 2 H), 1.51 - 1.68 (m, 2 H), 1.49 (s, 3 H), 1.31 - 1.46 (m, 1 H), 0.87 (s, 3 H) LC-MS (ESI POS): 577.29 MH+ [α]〇25 = + 122.1 (c 0.134, CHC13) [實施例9] 101108S88 123 201247697
(4&8,仆11,58,6&8,仙11,9&8,1(^,1058,128)-41),12-二氟_5_經 基-4a,6a-.一甲基-2-側氧基-8- °塞吩_2_武曱美 -2,4a,4b,5,6,6a,8,9,9a,10,l〇a,10b,11,12-H- izg Ιΐ-7-^.8.πγ_^ 搭烯并[2,1-a]菲-6b·羧酸氟甲基酯(化合物73)之製備 於化合物44 (150毫克,0.297毫莫耳)於無水DMF (3毫升) 之溶液内於氤氣環境下添加碳酸鈉(157毫克,1 483毫莫 耳)。於室溫攪拌20分鐘後,混合物冷卻至〇〇c及添加溴氟甲 烷(0.371毫升,0.742毫莫耳”反應混合物於〇艽攪拌15分鐘 及於室溫攪拌1小時;然後又添加溴氟曱烷(0 371毫升,〇 742 毫莫耳)於DMF之2 Μ溶液及混合物於室溫攪拌46小時。反 應混合物倒入冷鹽酸溶液(1毫升1 Ν鹽酸及19毫升水)内及 水相以乙酸乙酯(3x40毫升)萃取。組合有機萃取物經脫水 (硫酸納)及濃縮。粗產物(162毫克)以j)CM/AcOEt 97:3至 DCM/AcOEt 84:16之梯度洗提藉二氣化矽凝膠急速層析術 純化獲得92毫克純質化合物(58〇/。產率;尺产〇 39於 AcOEt/DCM 20:80)。 101108588 124 201247697 *H NMR (300 MHz, DMSO-d^) ppm 7.39 (dd, 1 H), 7.26 (dd, 1 H), 6.76 -7.02 (m, 2 H)a 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.76 (dd, 1 H), 5.89 (dd, 3 H), 5.53 -5.73 (m, 1 H), 5.50 (d, 1 H), 4.12 - 4.28 (m, 1 H), 4.10 (br. s., 2 H), 3.48 - 3.65 (m, 2 H), 2.56 - 2.70 (m, 1 H), 2.04 - 2.33 (m, 2 H), 1.83 - 2.04 (m, l H), 1.54 - 1.83 (m, 2 H), 1.50 (s, 3 H)s 1.35 - 1.48 (m, 1 H), 0.94 (s, 3 H) LC-MS (ESI POS): 538.28 MH+ [a]D25 = + 46.49 (c 0.111; CHC13) 表4列舉之化合物係如先前對化合物73所述利用適當烷化 劑製備: [表4] 化合物 結構式 產率 分折 74 64% LC-MS (ESI POS): 550.31MH+ []D25 =十 222.5 (c 0.064; CHCU) NMR (300 MHz, DMSO-de) ppm 7.27 - 7.35 (m, 2 H), 7.25 (ddf 1 H), 6.98 - 7.16 (m, 2 H), 6.29 (dd, 1 H), 6.12 (s, l H), 5.86 (dd, 1 H), 5.80 (dd, 1 H), 5.52 - 5.76 (m, 1 H), 5.50 (dd, 1 H), 4.09 - 4.24 (m· 1 H)· 3.92 (d, 1 H),3.84 (d, 1 H), 3.42 - 3.69 (m, 2 H), 2.55 - 2.71 (m, 1 H), 2.05 - 2.36 (m, 2 H), 1.77 -1.92 (m, 1 H), 1.53 - 1.77 (m,4H),l_49(s,3H),1.39 • 1.47 (m, 1 H),0.94 (s, 3 H) 75 F 75% LC-MS (ESI POS): 557.3 MH+ [b25 = + 112.3 (c 0.2 MeOH) lH NMR (300 MHz, DMSO-de) ppm 7.20 - 7.39 (m, 3 H), 7.09 (t, 2 H), 6.29 (dd, 1 H), 6.12 (s, 1 H), 5.54 - 5.79 (m, 1 H), 5.52 (d.1 H), 5.11 (d,lH), 5.05 (d, 1 H)9 4.08 - 4.22 (m» 1 H), 3.93 (d, 1 H), 3.82 (d, 1 H), 3.51 - 3.59 (m, 1 H), 2.53 - 2.63 (m, 1 H), 2.36 -2.45 (m, 1 H), 2.22 - 2.36 (m, 2 H), 2.04 - 2.21 (m, 1 H), 1.59 · 1-91 (m, 3 H), 1.33 - 1.59 (m, 2 H), 1.49 (s, 3 H), 0.93 (s. 3 H> 125 101108588 201247697 r LC-MS (ESI POS): 545.04 MH+ []d2S = + 74.80 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.35 - 7.42 (m,1 H),7.26 (dd,1 H), 37% 6.84 . 6.99 (m, 2 H), 6.30 76 Ρ (dd, 1 H), 6.12 (s, 1 H), 5.55 - 5.80 (m, 1 H), 5.50 - 5.55 (m, 1 H), 5.06 (s, 2 H), 4.12 - 4.28 (m,lH), 3.93- 4.12 (m, 2 H), 3.45 - 3.68 (m, 2 H)s 2.55 - 2.63 (in, 1 H), 2.02 - 2.33 (m, 3 H), 1.81 - 2.02 (m, 1 H), 1.59 - 1.81 (m,2H), 1.49 (s, 3 H), 1.32 - 1.47 (m, 2 H), 0.93 (s,3H) [實施例ίο]
(4&8,仆11,58,6&8,6匕11,9&8,1〇38,1(^8,128)-41),12-二氟-8-呋 D南-2-基曱基-5-經基-4a,6a-二甲基-2-侧氧基 -2,4&,41),5,6,63,8,9,9&,10,10&,101),11,12-十四氫-7-〇号_8_吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯(化合物77)之製備 化合物45 (453毫克,0.925毫莫耳)’HATU (387毫克,1.018 毫莫耳)及N-曱基咮啉(0.102毫升,0.925毫莫耳)於無水 DMF(15毫升)之混合物於氮氣環境下於70°C攪拌1.5小時, 及LC-MS顯示期望活性酯之形成(93%轉化率)。溶液冷卻至 至溫及添加無水硫化氫鈉(156毫克,2.78毫莫耳)。混合物於 101108588 126 201247697 室溫攪拌25分鐘’然後添加2M之溴氟曱烷(1.388毫升,2.78 毫莫耳)於DMF之溶液,及混合物於室溫授拌2小時。又添加 溴氟甲烷(0.463毫升,0.925毫莫耳)及反應混合物於室溫攪 \ 拌隔夜。 : 反應混合物以乙酸乙醋(130毫升)稀釋及有機相以水及鹽 水洗務,脫水(硫酸鈉)及濃縮。所得粗產物混合物(561毫克) 於乙酸乙酯/石油醚5:95至乙酸乙酯/石油喊30:70之梯度洗 k及然後使用DCM洗提於二氧化矽凝膠上藉急速層析術純 化獲得184毫克標題化合物(37%產率;r产〇 79於 AcOEt/DCM 30:70)。 Ή NMR (300 MHz, DMSO-d6) ppm 7.54 (dd, i H) ? 25 (dd { H) 6.26 - 6.41 (m, 3 H), 6.12 (s, 1 H), 5.88 (dd, 1 H), 5.78 (dd, i H) 5 51 5 75 (m, 1 H), 5.50 (dd, 1 H), 4.10 - 4.26 (m, 1 H), 3.95 (s, 2 H)j 3 ^ . 3 55 (m { H), 3.33 - 3.42 (m, 1 H), 2.56 - 2.69 (ra, 1 H), 2.02 、 ’
3H), 1.90 (dt, I H),1.50 - 1.77 (m,3 H), 1.49 (s, 3 H), 1.40 · 1.48 (ra,1 H)’ 〇 88 (s 3 印 LC-MS (ESI POS): 538.4 (MH+) ’ [a]D25 = + 112.4 (c 0.145; CHClj) 表5列舉之化合物壯先前對化合物77所述,始於適當酸 衍生物製備: 胃 ; [表 5] 127 101108588 201247697 化合物 結構式 產率 分析 78 参 86% LC-MS (ESI POS): 566.46 MH+ No25 = + 163.3 (c 0.174, CHC13) 'H NMR (300 MHz, DMSO-de) ppm 7.29 - 7.39 (m, 2 H), 7.24 (dd, 1 H), 7.04 - 7.16 (m, 2 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.86 (dd, 1 H), 5.76 (dd, 1 H), 5.52 - 5.74 (m, 1 H), 5.50 (dd, 1 H), 4.07 - 4.28 (m, 1 H), 3.95 (d, 1 H), 3.86 (d, 1 H), 3.46 - 3.61 (m, 1 H), 3.33 - 3.46 (m, 1 H), 2.56 -2.76 (m, 1 H), 2.04 - 2.31 (m, 3 H), 1.78 - 1.95 (m, 1 H), 1.51 - 1.74 (m, 4 H), 1.49(s,3H),0.88(s,3H) 79 β 39% LC-MS (ESI POS): 554.42 MH+ [a]D25 = +123.9 (c 0.108, CHC13) 'H NMR (300 MHz, DMSO-di) ppm 7.42 (dd, 1 H), 7.25 (dd, 1 H), 6.99 (dd, 1 H), 6.95 (dd, 1 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.88 (dd, 1 H), 5.78 (dd, 1 H), 5.53 - 5.76 (m, 1 H), 5.51 (dd, 1 H), 4.18 -4.21 (m, 1 H), 4.19 (d, 1 H), 4.12 (d, 1 H), 3.44 -3.58 (m, 1 H), 3.35 - 3.44 (m, 1 H), 2.58 - 2.75 (m, 1 H), 2.03 - 2.37 (m, 3 H), 1.86 - 2.03 (m, 1 H), 1.52 -1.79 (m, 3 H), 1.49 (s, 3 H), 1.38 - 1.48 (m, 1 H), 0.89 (s,3H) 128 101108588 201247697 80 F 16% LC-MS (ESI POS): 542.37 MH+ [a]D25 = + 134.9 (0.23, MeOH) 'H NMR (300 MHz, DMSO-ds) ppm 7.24 (d, 1 H), 6.29 (dd, l H), 6.12 (s, 1 H), 5.89 (dd, 1 H), 5.81 (dd, 1 H), 5.53 - 5.73 (m, 1 H), 5.50 (dd, 1 H), 4.07 -4.24 (m, 1 H), 3.46 - 3.67 (m, 1 H), 3.32 - 3.45 (m, 1 H), 2.55 - 2.78 (m, 3 H), 1.95 -2.33 (m,3H), 1.82- 1.95 (m, 1 H), 1.51 - 1.80 (m, 4 H), 1.49 (s, 3 H), 1.29 - 1.47 (m, 2 H), 0.89 (s, 3 H), 0.86 (s, 9 H) 81 F 11% LC-MS (ESIPOS): 568.14 MH+ [a]〇2S = +57.09 (c 0.27, DMF) 'H NMR (300 MHz, DMSO-de) ppm 7.25 (dd, 1 H), 6.75 (d, 1 H), 6.61 (dq, 1 H), 6.30 (dd, 1 H), 6.09-6.14 (m, 1 H), 5.89 (dd, 1 H), 5.79 (dd, 1 H), 5.51 - 5.75 (m, 1 H), 5.49 (dd, 1 H), 4.14-4.26(m, 1 H),4.10(d, 1 H), 4.04 (d, lH),3.31-3.50(m,2H), 2.56 - 2.70 (m, 1 H), 2.34 (d, 3 H), 2.02 - 2.30 (m, 3 H), 1.90-2.02(01,1 H), 1.72 (d, 1H), 1.51-1.67 (m, 1H), 1.49(s,3H), 1,31 - 1.48 (m,2 H), 0,89 (s,3If) 129 101108588 201247697 82 20% LC-MS (ESI POS): 578.1] MH+ [a]D25 = + 131.6 (c 0.25, CHC13) lHNMR(300 MHz, DMSO-de) ppm 7.25 (dd, 1 H), 7.14 - 7.22 (m, 2 H), 6.75 - 6.90 (m, 2 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.87 (dd, 1 H), 5.77 (dd, 1 H), 5.51 - 5.73 (m, 1 H)3 5.49 (dd, 1 H), 4.08 - 4.28 (m, 1 H),3.89(d, 1 H), 3.83 (d, 1 H), 3.71 (s, 3 H), 3.39 - 3.52 (m, 1 H), 3.32 -3.41 (m, 1 H), 2.55 -2.71 (m, 1 H), 2.03 - 2.37 (ra, 3 H), 1.82- 1.97 (m, 1 H), 1.52 - 1.75 (m, 3 H), 1.49 (s, 3 H), 1.40- 1.48 (m, 1 H), 0.88 (s, 3 H) 83 P 37% LC-MS (ESI POS): 528.2 MH+ [a]〇25 = + 132.9 (c 0.1145 CHCh) 'HNMR(300 MHz, DMSO-de) ppm 7.24 (dd, 1 H), 6.29 (dd, 1 H), 6.08 -6.18 (m, 1H), 5.89 (dd, 1 H),5.81 (dd, 1H),5.51 -5.73 (m, 1 H), 5.49 (dd, 1 H), 4.05 - 4.26 (m, 1 H), 3.45 - 3.66 (m, 1H), 3.31 - 3.45 (m,lH), 2.55-2.81 (m,3H), 2.19-2.36 (m, 1 H), 1.95 - 2.19 (m, 2 H), 1.79- 1.93(m,lH),1.67-1.77 (m,lH)s 1.51-1.67 (m, 3 H), 1.49 (s, 3 H), 1.43- 1.48 (m, 1 H), 1.40 (q, 2 H), 0.89 (s, 3 H), 0.84 (d, 3 H), 0.84 (d, 3 H) 130 101108588 201247697 LC-MS (ESI POS): 540.2 MH+ [a]D25 = + 149.8 (C 0.145, CHC13) 'HNMR(300MHz, DMSO-de) ppm 7.24 (d,1 - f H), 6.29 (dd, 1 H),6.11 (s. 10% 1 H), 5.89 (dd, 1 H), 5.82 84 Μ〇γτη.) w (dd, 1 H), 5.55 (tn, 1 H), rmv 5.49 (dd, 1 H), 3.99 - 4.28 F (m, 1 H), 3.44 - 3.65 (m, 1 H), 3.37 (m, 1 H), 2.56 -2.70 (m, 1 H), 2.54 - 2.70 (m,2H), 2.19-2.34 (m, 1 H), 1.98 - 2.19 (m, 3 H), 1.82- 1.98 (m, 1 H), 1.56-1.82 (m, 4 H), 1.37-1.56 (m,6H), 1.48 (s, 3 H), 0.98 - 1.24 (m, 2 H), 0.89 (s,3H) LC-MS (ESI POS): 590.18 MH十 [a]〇2S = + 84.95 (c 0.109, CHCI3) 'HNMR(300 MHz, DMSO-d«) ppm 7.24 (dd, r 1 H), 7.14-7.21 (m,2H), 7.05 - 7.14 (m, 2 H), 6.30 43% (dd, 1 H), 6.12 (s, 1 H), 85 5.88 (dd, 1 H), 5.77 (dd, 1 H), 5.50-5.74 (m, 1 H), f 5.48 (dd, 1 H), 4.08 - 4.24 (m, 1 H), 3.90 (s, 2 H), 3.32-3.51 (m, 2 H), 2.55-. 2.71 (m, 1 H), 2.43 - 2.48 (m, 2 H), 2.01 - 2.33 (m, 3 H), 1.82 -1.94 (m, 1H), 1.69 (d, 1 H), 1.50-1.65 (m, 4 H), 1.48 (s, 3 H), 1.36- 1.46 (m, 1H), 0.88 - (s, 3 H), 0.86 (t, 3 H) 131 101108588 201247697 86 F 14% LC-MS (ESI POS): 562.15 MH+ [a]D25 = +181.2(c 0.37, DMF) 'HNMR(300MHz, DMSOO ppm 7.24 (dd, lH),7.16(t,lH),7.1】-7.15 (m, 1 H), 6.98-7.10 (m, 2 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.89 (dd, 1 H), 5.80 (dd, 1 H), 5.51 -5.76 (m, 1 H), 5.49 (dd, 1 H), 4.07 - 4.28 (m, 1 H), 3.90 (s, 2 H), 3.42-3.54 (m, 1 H), 3.34 - 3.45 (m, 1 H), 2.56 - 2.71 (m, 1 H), 2.25 (s, 3 H), 2.02 - 2.24 (m,3H), 1.79- 1.94 (m, 1 H), 1.51 - 1.73 (m,4H), 1.49 (s,3H), 0.89 (s, 3 H) 87 F 31% LC-MS (ESI POS): 588.11 MH+ [a]D25 = + I55.6(c 0.43, DMF) 'H NMR (300 MHz, DMSO-de) ppm 7.25 (dd, 1 H), 6.94 (d, 1 H), 6.86 (d, 1 H), 6.30 (dd, 1 H), 6.12 (s, 1 H),5.88(dd, 1 H), 5.79 (dd, 1 H), 5.53 -5.76 (m, 1H), 5.51 (dd, 1 H), 4.16-4.25 (m, 1 H), 4.18 (d, 1 H), 4.02 (d, 1 H), 3.45 - 3.61 (m, 1 H), 3.35 - 3.46 (m, 1 H), 2.56 -2.70 (m, IH), 2.05-2.31 (m,3H), 1.85- 1.98 (ms 1 H), 1.68- 1.78 (m,lH), 1.53 - 1.68 (m, 2 H), 1.49 (s,3H), 1.39-1.47 (m,l H), 0.89 (s, 3 H) 132 101108588 201247697 88 r 10% LC-MS (ESI POS): 562.16 MH+ Wd25 = +145.2 (c 0.34, MeOH) 'HNMR(300MHz, DMSO-d6) ppm 7.24 (dd, 1 H), 7.15-7.21 (m,2H), 7.02 - 7.13 (m, 2 H), 6.30 (dd, 1 H), 6.09-6.15 (m, 1 H), 5.88 (dd, 1 H), 5.78 (dd, 1 H), 5.51 - 5.76 (m, 1 H), 5.49 (dd, 1 H), 4.09 -4.23 (m, 1 H), 3.91 (d, 1 H), 3.85 (d, 1 H), 3.41 -3.54 (m, 1 H), 3.34 - 3.42 (m, 1 H), 2.55-2.70 (m, 1 H), 2.26 (s, 3 H), 2.01 -2.25 (m, 3 H), 1.79-1.96 (m, 1 H), 1.49 (s, 3 H), 1.41 - 1.76 (m, 4 H), 0.88 (s,3H) rF LC-MS (ESI POS): 604.18 MH+ [a]D25 = +94.6 (c 0.0905, CHCI3) 'HNMR(300 MHz, DMSO-d^) ppm 7.27 -7.35 (m, 2 H), 7.24 (d, 1 a 5% H), 7.16 - 7.22 (m, 2 H), 89 6.30(dd, lH),6.U(s,l H), 5.90 (dd, 1 H), 5.79 (dd, 1 H), 5.52 - 5.69 (m,1 H), 4.07 - 4.28 (m, 1 H), 3.93 (s, 2 H), 3.31 -3.52 (m, 2 H), 2.54 - 2.70 (m, 1 H), 1.81 -2.37 (m, 5 H), 1.69(d, 1H), 1.53-1.65 (m, 1 fi), 1.48 (s, 3 H), 1.34- 1.46 (m, 2 H), 1.23 (s,9H), 0.88 (s, 3 H) 133 101108588 201247697 90 38% LC-MS (ESI POS): 594.2 MH+ [α]〇25 = +80.97 (c 0.103, CHC13) 'HNMR (300 MHz, DMSO-d«) ppm 7.05 -7.41 (m, 6 H), 6.30 (dd, 1 H), 6.11(8,1^,5.91 (dd, 1 H), 5.82 (dd, 1 H), 5.53 -5.73 (m, 1 H), 5.52 (dd, 1 H), 4.01 -4.36 (m, 1 H), 3.46 - 3.63 (m, 1 H), 3.33 - 3.46 (m, 1 H), 3.13-3.23 (m, 1 H), 3.03-3.13 (m, 1 H), 2.94 - 3.03 (m, 1 H), 2.80 - 2.94 (m, 1 H), 2.55 -2.68 (m, 1 H), 2.01 - 2.36 (m,3H), 1.81 -2.01 (m, 1 H), 1.53 -1.81 (m, 3 H), 1.49 (s, 3 H),1.38-1.48 (m, 1 H), 0.90 (s, 3 H) 91 Ρ 15% LC-MS (ESI POS): 556.26 MH+ [a]D25 = + 137.9 (c 0.2 MeOH) 'HNMR (300 MHz, DMSO-de) ppm 7.24 (dd, 1H), 6.29 (dd, 1H), 6.11 (s, 1 H), 5.90 (dd, 1 H), 5.81 (dd, 1 H), 5.51 -5.71 (m, 1 H), 5.49 (dd, 0 H), 4.04 - 4.27 (m, 1 H), 3.42 -3.59(1X1, 1 H), 3.32-3.42 (m, 1 H), 2.56 - 2.70 (m, 2 H), 1.97 - 2.32 (m,4 H), 1.82 - 1.96 (m, 1 H), 1.69-1.80 (m, 1H), 1.51-1.69 (m,3H), 1.49 (s,3H), 1.13 - 1.47 (m, 8 H), 0.88 (s, 3 H), 0.85 (t, 3 H), 0.83 (t,3H) 134 101108588 201247697 92 14% LC-MS (ESI POS): 578.2 MH+ [α]〇25 = + 131.1 (c 0.28, CHC!3) 'HNMR(300MHz, DMSO-de) ppm 7.17 -7.34 (m, 3 H), 6.82 - 7.01 (m, 3 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.86 (dd, t H), 5.73 (dd, 1 H), 5.53 -5.74 (m, 1 H), 5.51 (dd, 1 H), 4.15-4.31 (m, 1 H), 4.14 (t, 2 H), 3.51 -3.71 (m, 1 H), 3.33 - 3.51 (m, 1 H),3.13-3.24(m, 1 H), 2.96-3.13(m, 1 H), 2.55-2.76 (m, 1 H), 2.04 - 2.35 (m,3H), 1.82- 1.97 (m,l H), 1.S1 - 1.80 (m, 4 H), 1.49 (s, 3 H), 0.90 (s, 3 H) 93 32% LC-MS (ESI POS): 572.13 MH+ [a]D25 = + 148.7 (c 0.33, DMF) 'HNMR(300MHz, DMSO-φι) ppm 7.24 (dd, 1 H), 6.42 (d, 1 H), 6.37 (d, 1 H), 6.30 (dd, 1 H), 6.12 (s, 1 H), 5.87 (dd, 1 H), 5.77 (dd, 1 H),5.51 - 5.76 (m, 1 H), 5.49 (dd, 1 H), 4.07 - 4.27 (m, 1 H), 3.96 (d, 1 H), 3.86 (d, 1 H), 3.45 - 3.58 (m, 1 H), 3.34 3.45 (m, 1 H), 2.57 -2.71 (m, 1 H), 1.98-2.32 (m,3H), 1.83- 1.94 (m, l H),1.49(s,3H), 1.42- 1.76 (m, 4 H), 0.88 (s, 3 H) 135 101108588 201247697 101108588 94 95
136 21% 23% LC-MS (ESI POS): 540.27 MH+ [ct]D25 =十 126.8(c0.2 MeOH) 'ΗΝΜΚ(300ΜΗζ, DMSO-de) ppm 7.24 (dd, 1 H),6.29(dd, 1 H), 6.11 (s, 1 H), 5.89 (dd, 1 H), 5.79 (dd, 1 H), 5.51 - 5.75 (m, 1 H), 5.49 (dd, 1 H), 4.01 - 4.26 (m, 1 H), 3.43 -3.64 (m, 1 H), 3.31 - 3.42 (m, 1 H), 2.55 - 2.71 (m, 2 H), 2.19-2.35 (m, I H), 1.95 - 2.19 (m, 3 H), 1.81 - 1.95 (m,l H), 1.52- 1.78 (m,7H), 1.49 (s,3H), 1.40-1.48(m, 1 H), 1.01 -1.36(m,5 H), 0.89 (s, 3 H) LC-MS (ESI POS): 542.05 MH+ [a]〇2s = + 167.0 (c 0.2, CHCb) *HNMR(300 MHz, DMSO-de) ppm 7.24 (dd, 1 H), 6.29 (dd, 1 H),6.11 (s, 1 H), 5.89 (dd, 1 H), 5.82 (dd, 1 H), 5.50 - 5.72 (m, 1 H), 5.49 (dd, 1 H), 4.08 - 4.26 (m, 1 H), 3.43 -3.59 (m, 1 H), 3.33-3.43 (m, 1 H), 2.61-2.70 (ra, 1 H), 2.58 (t, 2 H), 1.98 -2.36 (m, 3 H), 1.80-1.94 (m, 1 H), 1.51 - 1.77 (m, 5 H), 1.49 (s,3H), 1.39-1.48 (m,lH), 1.13-1.36 (in, 3 H), 0.89 (s, 3 H), 0.81 (t, 3 H), 0.78 (t, 3 H) 201247697 LC-MS (ESI POS): 620.19 MH+ [ct]D25 = + 128.8 (c 0.105, CHC13) r 'H NMR (300 MHz, DMSO-d^) ppm 7.24 (dd, ( 1 H), 7.13-7.21 (m,2H), :‘ 16% 6.81 -6.90(m?2H), 6.30 96 (dd,1 H),6_] 1 (s,1 H), rmP 5.86 (dd, l H), 5.75 (dd, 1 F H), 5.49 - 5.75 (m, 1 H), 5.48 (dd, 1 H), 4.10-4.24 (m, 1 H), 3.94 (d, 1 H)s 3.87 (d, 1H), 3.31 -3.50 (m, 2 H), 2.54 - 2.72 (m, 1 H), 1.95 - 2.32 (m, 3 H), 1.82- 1.95 (m,l H), 1.51 -1.75 (m, 3 H), 1.48 (s, 3 H), 1.34- 1.46 (m,lH), 1.24 (s, 9 H), 0.88 (s, 3 H) LC-MS (ESI POS): 620.24 MH+ [a]D25 = + 142.4 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-dfi) ppm 7.25 (dd, rF Λ λ 1 H), 7.12-7.21 (m,2H), 6.76 - 6.87 (m, 2 H), 6.30 27% (dd,lH)}6.12(s,lH), PV. 97 ί 5.88 (dd, 1 H), 5.77 (dd, 1 H), 5.51 -5.75 (m, 1 H), 5.49 (dd, 1 H), 4.09 - 4.26 (m, 1 H), 3.91 (t, 2 H), 3.89 (br. s., 1 H), 3.83 (d, 1 H), 3.32 - 3.50 (m, 2 H), 2.56-2.71 (m, 1 H),2.01 -2.35 (m, 3 H), 1.81 -1.98 (m,lH), 1.53 - 1.77(m,5 H), 1.49 (s, 3 H), 1.34 - 1.47 (m, 3 H), 0.93 (t, 3 H), 0.88 (s, 3 H) 137 101108588 201247697 98 18% LC-MS (ESI POS): 552.2 MH+ [α]〇25 = + 104.3 (c 0.6, CHC13) 'HNMR (300 MHz, DMSO-de) ppm 7.25 (dd, 1H), 6.30(dd, 1H), 6.18 (d, 1 H), 6.12 (s, 1 H), 5.96 (dq, 1 H), 5.88 (dd, 1 H), 5.79 (dd, 1 H),5.51 -5.76 (m, 1 H)f 5.49 (dd, L H), 4.09-4.26 (m, 1 H), 3.92 (d, 1 H), 3.85 (d, 1 H)s 3.40-3.52 (m, 1 H),3.33-3.42 (m, 1 H), 2.57 - 2.70 (m, 1 H), 2.20 - 2.26 (m, 1 H), 2.18 (d, 3 H), 2.01 -2.16 (m, 2 H), 1.83 -1.96 (m, 1 H), 1.52 - 1.77 (m, 3 H), 1.49 (s, 3 H), 1.37-1.48 (ra, 1 H), 0.88 (s, 3 H) 99 16% LC-MS (ESI POS): 599.88 MH+ [a]D25 = +115.9 (c 0.162, CHC13) 'HNMR(300 MHz, DMSO-de) ppm 7.25 (dd, 1 H), 6.95 (d, 1 H), 6.87 (d, 1 H), 6.30 (dd, 1 H), 6.11 (s, 1 H),5.89(dd, 1 H), 5.79 (dd, 1 H), 5.52 -5.72 (m, 1 H), 5.50 (dd, 1 H),4.19(d, 1 H),4.15 -4.21 (m, 1 H), 4.08 (d, 1 H), 3.33 - 3.52 (m, 2 H), 2.54 - 2.70 (m, 1 H), 2.37 (s, 3 H), 2.04 - 2.30 (m, 3 H), 1.89 - 2.03 (m, 1 H), 1.68- 1.79 (m, 1 H), 1.52-1.68 (m, 1 H), 1.49 (s, 3 H), 1.35- 1.47 (m, 2 H), 0.89 (s, 3 H) 138 101108588 201247697 100 19% LC-MS (ESI POS): 542.18 MH+ [<x]D25 = + 143.9 (c 0.25, MeOH) *HNMR(300MHz, DMSO-d6) ppm 7.24 (dd, 1 H), 6.29 (dd, 1H), 6.11 (s, 1 H), 5.79 - 6.03 (m, 1 H), 5.71 -5.94 (m, 1 H), 5.51 - 5.73 (m, 1 H), 5.49 (dd, 1 H), 4.18 (dd, 1 H), 3.51 (t, 1 H), 3.32 - 3.45 (m, 1 H), 2.58 - 2.70 (m, 1 H),2.01 -2.35(m,5H), 1.83-2.01 (m, 1 H), 1.56-1.83 (m, 4 H), 1.49 (s, 3 H), 1.43-1.56 (m,2H), 0.97 (t, 3 H), 0.80 - 0.93 (m, 7 H), 0.75 (d, 2 H) 101 放' F 18% LC-MS (ESI POS): 554.02 MH+ [α]〇25 = + 129.0 (c 0.111, CHCb) *HNMR(300 MHz, DMSO-de) ppm 7.24 (dd, 1 H), 6.29 (dd, 1 H), 6.12 (s, 1 H), 5.90 (dd, 1 H), 5.82 (dd, 1 H), 5.56 (m, 1 H),5.51(m, 1H),3.98-4.30 (m, 1 H), 3.49 - 3.73 (m, 1 H), 3.34 - 3.47 (m, 1 H), 2.96-3.17 (m, 1 H), 2.76 - 2.93 (m, 1 H), 2.55 -2.69 (m, 1 H), 2.21 - 2.32 (m, 2 H), 2.02 - 2.20 (m, 2 H),1.89(dt,lH),1.54-1.80 (m, 4 H), 1.43-1.53 (m, 1 H), 1.49 (s, 3 H), 0.90 (s, 3 H) 139 101108588 201247697 102 f 17% LC-MS (ESI POS): 512.12 MH+ [a]〇2S = +129.6 (c0.25, MeOH) 'HNMR(300 MHz, DMSO-de) ppm 7.24 (d, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.90 (dd, 1 H), 5.80 (dd, 1 H),5.51 -5.77 (m, 1 H),5.49(dd, 1 H),4.16(d, 1 H), 3.46-3.66 (m,lH), 3.31 - 3.46 (m, l H), 2.60- 2.80 (m, 2 H), 2.60 - 2.75 (m, 1 H), 2.19-2.36 (m, 1 H),2.01 -2.19(m,2H), 1.81 -1.96 (m, 1 H), 1.55- 1.81 (m, 2 H),1.49 (s, 3 H), 1.34- 1.55 (m, 2 H), 0.78 - 0.99 (m, 1 H), 0.90 (s, 3 H), 0.27 - 0.59 (m, 2 H), -0.06 - 0.27 (m, 2 H) 103 29% LC-MS (ESI POS): 568.23 MH+ [a]〇25 = + 172.6 (c 0.21, MeOH) 'HNMR(300 MHz, DMSO-de) ppm 7.24 (dd, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.89 (dd, 1 H), 5.81 (dd, 1 H), 5.51 -5.71 (m, 1 H), 5.49 (dd, 1 H), 4.02 - 4.26 (m, 1 H), 3.45 -3.66 (m, 1 H), 3.31 - 3.45 (m, 1 H), 2.55 - 2.82 (in, 3 H), 2.17-2.33 (m, 1 H), 1.95 - 2.17 (m, 2 H), 1.81 -1.94(m,lH), 1.52-1.78 (m,8H), 1.49(s,3 H), 1.26- 1.47 (m, 4 H), 1.00-1.24 (m,3 0.89 (s, 3 H), 0.70 - 0.86 (m, 2 H) 140 101108588 201247697 104 19% LC-MS (ESI POS): 552.22 MH+ [α]〇25 = + 150.4 (c 0.24, MeOH) 'HNMR (300 MHz, DMSO-de) ppm 7.24 (d, 1 H),6.29(dd, 1H),6.11 (s, 1 H), 5.91 (dd, 1 H), 5.83 (dd,1 H),5.51 - 5.75 (m, 1 H),5.50(dd,lH),3.51-3.69 (m, 1 H), 3.41 (q, 1 H), 2.54 - 2.87 (m, 2 H), 1.51 -2.36 (m, 11 H), 1.49 (s, 3 H), 0.95 - 1.46 (m, 7 H), 0.87 (s,3H), 0.51 -0.75 (m, 1 H) 105 F 7% LC-MS (ESI POS): 601.08 MH+ [a]〇2S = +76.63 (c 0.16 DMF) · lHNMR(300 MHz, DMSO-d^) ppm 7.55 (dt, 1 H), 7.37 (d, 1 H), 7.20 -7.30 (m, 2 H), 7.12 (ddd, 1 H), 6.98 (ddd, 1 H), 6.32 (dd, 1 H), 6.13 (s, 1 H), 5.91(dd, lH),5.81(dd, 1 H), 5.53 - 5.77 (m, 1 H), 5.51 (dd, 1 H), 4.10-4.38 (m, 2 H), 3.84 - 4.03 (m, 1 H), 3.71 (s, 3 H), 3.33 -3.41 (m, 2 H), 2.55 - 2.68 (m, 1 H), 2.10 - 2.34 (m, 3 H), 1.92-2.03 (m, 1 H), 1.53 - 1.86 (m, 3 H), 1.50 (s, 3 H), 1.38- 1.48 (m, 1 H), 0.90 (s, 3 H) [實施例11]
(6S,8S,9R,10S,llS,13S,14S)-6,9-二氟-17-(2-氟-乙醯 141 101108588 201247697 基)-11-經基·10,13-二曱基_6,7,8,9,10,u,12,13,14,15_+;4、 環戊[a]菲-3-酮(中間產物1〇6)之製備 於化合物6 (0.5克’ 1.321毫莫耳)於無水乙腈(2〇毫升)之溶 液内於氮氣環境下添加DIPEA (0.396毫升,2.246毫莫耳)及 Ms-Cl (0.155毫升,1.982毫莫耳)及反應混合物於室溫攪拌1 小時。然後添加7^入?(2.64毫升’2.64毫莫耳)114於!'1^及 氟化鉀(0.077克,1,321毫莫耳)及混合物回流加熱隔夜。混 合物以乙酸乙酯稀釋及有機相以水、鹽水洗滌,脫水(硫酸 鈉)及濃縮。粗產物於石油醚/乙酸乙酯8:2至乙酸乙酯之梯度 洗提’於二氧化梦凝膠上藉急速層析術純化獲得標題化合物 (98%產率)。 LC-MS (ESI POS) : 381.3 ΜΗ (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二戴 -6b-(2-氟-乙醯基)-5-經基-4a,6a-二曱基-8-(4-甲基.节 基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-o号-8-吖-戊搭烯并[2,l-a]菲-2-酮(化合物107)之製備 如先前對化合物1〇(實施例4)所述,化合物107係經由中間 產物40與N-(4-曱基-节基)-羥基胺反應而以48%產率獲得。 101108588 142 201247697 'lH NMR (300 MHz, DMSO-d6) ppm 7.27 (dd, 1 H), 7.03 - 7.22 (m, 4 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.49 - 5.79 (m, 1 H), 5.45 (d, 1 H), 4.89 (d, 2 H), 4.07 - 4.29 (m, 1 H), 3.87 (d, 1 H), 3.76 (d, l H), 3.40 - 3.61 (m, 1 H), 3.31 - 3.40 (m, 1 H), 2.55 - 2.68 (m, 1 H), 2.28 (s, 3 H), 2.02 - 2.27 (m, 3 H), 1.74 - 1.96 (m, 1 H), 1.51 - 1.73 (m, 3 H), 1.49 (s, 3 H), 1.46 (dd, 1 H), 0.84 (s, 3 H) LC-MS (ESI POS): 530.25 MH+ J [aJD25 = + 176.3 (c = 0.1715, CHClj) 表6列舉之化合物係如先前對化合物4i i〇7所述,經由中 間產物106與適當羥基胺或羥基胺鹽酸鹽之環化加成製備。 [表6] 化合物 結槐式 產牟 分析 LC-MS (ESI POS): 506.19 MH+ Wd25 = + 180.8 (c 0.2 MeOH) 'H NMR (300 MHz, F DMSO-de) ppm 7.59 (dd, l H), 7.27 (dd, 1 H), 6.41 108 43% (dd, 1 H), 6.25 - 6.35 (m, 2 H), 6.12 (s, l H), 5.49 - A 5.80 (m, 1 H), 5.46 (dd, 1 H), 5.00 (d, 2 H), 4.09 -4.26 (m, 1 H), 3.98 (d, 1 H), 3.84 (d, 1 H), 3.41 -3.61 (m, 1 H), 3.31 - 3.41 (m, 1 H), 2.56 - 2.70 (m, 1 H), 2.03 - 2.33 (m, 3 H), 1.79 - 1.96 (m, 1 H), 1.50 -1.70 (m, 3 H), 1.49 (s, 3 H), 1.44 (dd, 1 H), 0.85 (s, 3 H) 143 101108588 201247697 109 30% LC-MS (ESI POS): 534.27 MH+ [a]D25 = + 157.4 (c 0.2 MeOH) H NMR (300 MHz, DMSO-de) ppm 7.30 - 7.38 (m, 2 H), 7.27 (dd, 1 H), 7.07 - 7.21 (m, 2 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.48 - 5.83 (m, 1 H), 5.45 (m, 1 H), 4.90 (dd, 1 H), 4.80 (dd, 1 H), 4.16 (m, 1 H), 3.93 (d, 1 H), 3.79 (d, 1 H), 3.44 - 3.60 (m, 1 H), 3.25 - 3.43 (m, 1 H), 2.56 -2.70 (m, 1 H), 2.10 - 2.32 (m5 3 H), 1.79 - 1.97 (m, 1 H), 1.52 - 1.71 (m, 3 H), 1.49 (s, 3 H), 1.40 - 1.47 (m, 1 H), 0.84 (s, 3 H) 110 F 79% LC-MS (ESI POS): 506.19 MH+ [a]D25 = + 180.8 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.59 (dd, 1 H), 7.27 (dd, 1 H), 6.41 (dd, 1 H), 6.25 - 6.35 (m, 2 H), 6.12 (s, 1 H), 5.49 -5.80 (ra, 1 H), 5.46 (dd, 1 H), 5.00 (d, 2 H), 4.09 -4.26 (m, 1 H), 3.98 (d, 1 H), 3.84 (d, 1 H), 3.41 -3.61 (m, 1 H), 3.31 - 3.41 (m, 1 H), 2.56 - 2.70 (m, 1 H), 2.03 - 2.33 (m, 3 H), 1.79 - 1.96 (m, 1 H), 1.50-1.70(m,3H),1.49(s,3 H), 1.44(dd,〗 H),0.85(s,3H) 144 101108588 201247697 111 54% LC-MS (ESI POS): 546.23 MH+ [a]D25 = + 189.2 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.27 (dd, 1 H), 7.12 - 7.24 (m, 2 H), 6.79 - 6.94 (m, 2 H), 6.30 (dd, 1 H), 6.13 (s, 1 H), 5.50 - 5.79 (m, 1 H), 5.45 (dd, 1 H), 4.89 (d, 2 H), 4.12 - 4.25 (m, 1 H), 3.85 (d, 1 H), 3.73 (s, 3 H), 3.75 (d, 1 H), 3.39 - 3.54 (m, 1 H), 3.30 - 3.38 (m, 1 H), 2.55 - 2.68 (m, 1 H), 2.04 -2.33 (m, 3 H), 1.80 - 1.96 (m, 1 H), 1.51 - 1.71 (m, 3 H), 1.49 (s, 3 H), 1.45 (dd, 1 H), 0.84 (s, 3 H) 112 33% LC-MS (ESI POS): 508.3 MH+ [a]D25 = + 147.6 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.26 (dd, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.49 - 5.82 (m, 1 H), 5.45 (dd, 1 H), 5.29 (dd, 1 H), 5.17 (dd, 1 H), 4.00 -4.28 (m, 1 H), 3.53 (dt, 1 H), 3.31 - 3.43 (m, 1 H), 2.56 - 2.68 (m, 3 H), 1.83 -2.43 (m, 6 H), 1.51 - 1.77 (m,6H), 1.49(s,3H), 1.35 -1.47 (m, 3 H), 1.06-1.29 (m, 2 H), 0.86 (s, 3 H) 145 101108588 201247697 113 F 27% LC-MS (ESI POS): 510.31 MH+ [α]〇25 = + 118.3 (c 0.25, CHC13) 'H NMR (300 MHz, DMSO-de) ppm 7.26 (dd, 1 H), 6.29 (dd, 1 H), 6.11 (s, 1 H), 5.49 - 5.79 (m, 1 H), 5.46 (d, 1 H), 5.30 (dd, 1 H), 5.17 (dd, 1 H), 4.04 -4.29 (m, 1 H), 3.54 (t, 1 H), 3.31-3.40 (m, 1 H), 2.55 -2.86 (m, 3 H), 2.06 - 2.34 (m, 2 H), 1.82 - 2.03 (m, 2 H), 1.52 - 1.75 (m, 2 H), 1.49 (s, 3 H), 1.39 - 1.48 (m, 3 H), 1.22 - 1.38 (m, 1 H), 0.86 (s, 9 H), 0.86 (s, 3 H) 114 • 42% LC-MS (ESI POS): 556.14 MH+ [a]D25 = + 185.0 (c 0.2 MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.27 (dd, 1 H), 6.97 (d, l H), 6.87 (d, 1 H), 6.30 (dd, 1 H), 6.12 (s, I H), 5.50 - 5.79 (m, 1 H), 5.47 (d, 1 H), 5.15 (dd, 1 H), 5.04 (dd, 1 H), 4.15 -4.21 (m, 1 H), 4.19 (d, l H), 3.96 (d, 1 H), 3.44 -3.58 (m, 1 H), 3.31 - 3.44 (m, 1 H), 2.55 - 2.67 (m, 1 H), 2.05 - 2.25 (m, 3 H), 1.84 - 1.98 (m, 1 H), 1.63-1.73 (m, 1 H), 1.51 - 1.63 (m, 1 H), 1.49 (s,3H), 1.38 -1.47 (m, 2 H), 0.85 (s, 3 H) [實施例12] 146 101108588 201247697
(4&8,仆11,53,6&3批11,938,1(^,1(^8,128)_41),12-二氟-5-經 基-6b-(2-羥基-乙醯基)_8-[4-(2-第三丁基·二曱基-曱矽烷基 氧基-乙氧基)-苄基]·4&,6&_二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+i5^-7,《m 戊搭烯并[2,l-a]菲-2-酮(中間產物115)之製備 於化合物22 (200毫克,0.311毫莫耳)於無水DMF (8毫升) 之溶液内,於氮氣環境下,添加碳酸铯(223毫克,0.683毫 莫耳)’(2-溴乙氧基)(第三丁基)二甲基矽烷(135微升,〇 621 毫莫耳)及碘化鉀(10毫克,0.066毫莫耳)。反應混合物於5〇。匚 加熱隔夜’及又添加碳酸鉋(0.056克,0.171毫莫耳)及(2-溴 乙氧基)(第三丁基)二甲基矽烷(0.033毫升,0.155毫莫耳)。 然後混合物又於5 0 C擾摔8小時。反應混合物以乙酸乙醋稀 釋,有機相以水洗滌,以硫酸鈉脫水及濃縮。殘餘物於DCM 至DCM/AcOEt 7:3梯度洗提,於二氧化矽凝膠上藉急速層析 術純化獲得256毫克(92%產率)。 101108588 147 201247697 LC-MS (ESI POS):802.4 (MH+) (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-經 基-6b-(2-羥基-乙醯基)-8-[4-(2-羥基-乙氧基)-¥&]-4a,6a-二 曱基-4&,413,5,6,63,61),8,9,93,10,10&,1013,11,12-十四氫-7“等-8-吖-戊搭烯并[2,l-a]菲-2-酮(化合物116)之製備 於化合物115(0.256克,0.319毫莫耳)於無水THF (8毫升) 之溶液内於0°C於氮氣環境下添加氟化四丁基銨(〇·670毫 升’ 0.670毫莫耳)及混合物於〇°〇攪拌1小時及於室溫攪拌15 小時。溶劑經蒸發去除及粗產物(53 5毫克)以DCM/AcOEt 9·. 1 至AcOEt/EtOH 9:1之梯度洗提’於二氧化矽凝膠上藉急速層 析術純化。所得產物於DCM/AcOEt 6:4至AcOEt/EtOH 97.3 之梯度洗提’於二氧化石夕凝膠上藉急速層析術再度純化獲得 46毫克標題化合物(25°/。產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.26 (dd, 1 Η), 7.Π . 7 22 (m 2 H), 6.76 - 6.91 (m, 2 H), 6.30 (dd, 1 H), 6.13 (st 1 H), 5.50 - 5.74 (m, 1 H), 5.43 (dd, 1 H), 4.80 (t, 1 H), 4.65 (s, 1 H), 4.04 - 4.25 (m, 1 H)} 3.92 - 4.01 (m, 2 H), 3.60 - 3.90 (m, 5 H), 3.32 - 3.56 (m, 2 H), 2.56 - 2.68 (m, 1 H), 1.83 - 2.44 (m, 5 H), 1.51 - 1.68 (m, 3 H), 1.49 (s, 3 H), 1.37 -1.47 (m, 1 H), 0.80 (s, 3H) , , LC-MS (ESI POS): 574.39 (MH+) [a]D25 = + 155.8 (c 0.2 MeOH) [實施例13]
11$ 101108588 148 201247697 N-(4-氯苯基)羥基胺(中間產物1丨8)之製備 於1-氣-4-石肖基苯in (1克,6.35毫莫耳)於絕對乙醇(32毫 升)及水(10.24毫升)之分散液内,添加氣化站克, 1.269毫莫耳);然後’於水浴中,於氮氣環境下以攪拌徐缓 添加硼氩化鉀(0.514克,9.52毫莫耳)。混合物轉成黑色及形 成黑色沈澱。於室溫於氮氣環境下攪拌20分鐘後,混合物以 0.5 N鹽酸酸化至pH 7及即刻以乙醚萃取。有機萃取物以硫 酸鈉脫水及濃縮獲得期望之羥基胺(959毫克),其未經進一 步純化即就此使用。 LC-MS (ESI POS): 126.9 (MH+) [實施例14]
乙酸 2-((68,911,108,118,138)-6,9-二氟-11-羥基-1〇,13-二曱 基-3-側氧基 _6,7,8,9,10,11,12,13,14,15-十二氫-311-環戊[^]菲 -17-基)-;2-侧氧基-乙基酯(中間產物12〇)之製備 於丁酸(9尺,105,115,138,17幻-17-(2-乙醯氧基-乙醯基)-9_ 氯-11-經基-10,13-二甲基_3_側氧基 -6,7,8,9,10,11,12,13,14,15,16,17-十二氫-3仏環戊[3]菲-17-基 醋(中間產物119)(2.48克,4.88毫莫耳)於無水DMF (60毫升) 之溶液内於氮氣環境下添加乙酸鉀(3.83克,39.0毫莫耳)及 101108588 149 201247697 反應混合物於l〇〇°c攪拌i 5小時。冷卻後之反應混合物倒入 冰及鹽水(200毫升)内,及水層以乙酸乙酯(3xl5〇毫升)萃 取。組合有機萃取物以水及食鹽水洗滌,以硫酸鈉脫水及濃 縮獲得2.55克粗產物標題化合物’其未經進一步純化即用於 次一步驟。 H NMR (300 MHz, DMSO-i/e): ppm 7.29 (dd, 1 H), 6.99 (dd, 1 H), 6.29 (dd, 1 H), 5.98 - 6.15 (m, 1 H), 5.68 (dddd, 1 H), 5.56 (dd} 1 H), 5.10 (d, 1 H), 4.92 (d, 1 H), 3.98 - 4.23 (m, 1 H), 2.56 - 2.83 (m, 1 H), 2.26 - 2.44 (m,3 H),2.14 _ 2.26 (m, 1 H),2.09 (s,3 H),1.71 - 1.87 (m,1 H), 1.55 - 1.65 (m, 2 H), 1.53 (S> 3 H), 1.15 (s, 3 H). LC-MS (ESI POS): 421.97 (MH+) (68,911,1〇8,118,138)-6,9-二氟-11-羥基_17_(2_經基_乙酿 基)-l〇,13-二曱基七^爪^^以以十二氫-環戊㈤ 菲-3-酮(中間產物121)之製備 於(中間產物120)(2.55克,6.06毫莫耳)於乙醇(1〇〇毫开)之 溶液内,添加南極念珠菌脂解酶(2單位/毫克)(51〇毫克,6 〇6 毫莫耳)及反應混合物於37°C攪拌隔夜。反應混合物鎳過 濾,以甲醇洗滌’及殘餘物於DCM/Ac〇Et 9⑴1〇矣 DCM/AcOEt 50:50之梯度洗提,於二氧化矽凝膠上藉急速詹 析術純化獲得1.6 2克標題化合物(7 0.6 %產率)。 'H NMR (300 MHz, DMS0-rf6): ppm 7.29 (dd, 1 H), 6.87 (dd 1 H) 6-29 (dd, 1 H), 6.09 - 6.17 (m, 1 H), 5.67 (dddd, 1 H), 5.53 (dd, 1 H), 4.77 (t, 1 H), 4.44 (dd, I H), 4.26 (dd, 1 H), 4.04 - 4.15 (nis , H), 2.56 - 2.79 (m, 1 H), 2.39 (dd, I H), 2.25 - 2.35 (m, 2 H), 2.09 - 2.25 (m, 1 H), 1.76 (td, 1 H), 1.55 - 1.66 (m> 2 H), 1.53 (s, 3 H), 1.17 (s, 3 H). ’ LC-MS (ESI POS): 379.99 (MH+) 150 101108588 201247697 [實施例15]
(^SAbR^SMS^bR^aSAOaSAObSMS^b^-^-^-S-m 基-6b-(2-經基-乙酿基)_4a,6a-二曱基_8·苯基 -4江,41),5,6,6&,61),8,9,9牡,10,1〇3,101),11,12-十四氫_7_1|等_8-〇丫- 戊搭烯并[2,l-a]菲-2-酮(化合物122)之製備 121、N_苯基羥基胺(57.7毫克,0.529毫莫耳)及三聚曱搭 (47.6毫克’ 1,586毫莫耳)於乙醇(6毫升)之混合物於!〇〇〇〇擾 拌19小時。反應不完全。添加N-苯基羥基胺(2〇毫克,0.183 毫莫耳)及三聚甲醛(27毫克,0.899毫莫耳)及反應混合物又 於100°C加熱3小時。蒸發去除溶劑及殘餘物於DCM至 AcOEt/MeOH/DCM 9.8:0.2:90 至 Ac〇Et/MeOH/DCM 29.8:0.2:70之梯度洗提’藉二氧化石夕凝膠急速層析術純化獲 得83毫克純質化合物(63%產率;Rf=0.24於 AcOEt/MeOH/DCM 29:1:70)。 NMR (300 MHz,DMSO-d6) ppm 7.19 - 7 36 (m,3 H),6 9〇 · 7.04 (m, 3 Η), 6.28 (dd, 1 Η), 6.08 (s, 1 Η), 5.52 - 5.79 (m, 1 Η), 5.51 (dd, 1 Η), 4.92 (t,1 H),4.51 (dd,1 Η), 4.29 (dd,1 H),4.17 · 4.24 (m, 1 H),4.13 (t,1 H), 3.50 - 3.66 (m,1 H),2.61 - 2.71 (m,1 H),2.57 (dd, 1 H),2 0‘1 2.35 (in, 3 H), 1.51 - 1.82 (m, 4 H), 1.50 (s, 3 H), 0.91 (s, 3 H) LC-MS (ESI POS): 500.17 MH+ [a]D25 = + 71.09 (c 0.092; CHClj) 151 101108588 201247697 表7列舉之化合物係如先前對化合物122所述藉中間產物 121與適當羥基胺、羥基胺鹽酸鹽或經保護之羥基胺之環化 加成製備。於後述情況下,對終化合物進行脫保護反應。 終化合物係藉二氧化矽凝膠管柱層析術或製備性HPLC純 化。 [表7] 化合物 結構式 產率 分析 123 83% LC-MS (ESI POS): 534.19 MH+ [α]〇25 = + 72.74(c 0.19; CHC13) 'H NMR (300 MHz, DMSO-de) ppm 7.29 - 7.38 (m, 2 H), 7.25 (dd, 1 H), 6.93 - 7.05 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.52 - 5.77 (m, 1 H), 5.51 (d, 1 H), 4.94 (t, 1 H), 4.48 (dd, 1 H), 4.28 (dd, 1 H), 4.17-4.24 (m,lH), 4.13 (t, 1 H), 3.59 (q, 1 H), 2.60-2.69 (m, 1 H), 2.59 (dd, 1 H), 2.00 - 2.32 (m, 3 H), 1.51-1.83 (m, 4 H), 1.49 (s, 3 H), 0.90 (s, 3 H) 124 k 60% LC-MS (ESI POS): 514.22 MH+ [a]D25 = +81.8 (c 0.125, CHCI3) 'H NMR (300 MHz, DMSO-d6) ppm 7.26 (d,lH), 7.09. (m, 2 H), 6.87 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H),5.51 -5.78 (m, 1 H),5.31 - 5.52 (m, 1 H), 4.39 - 4.60 (m, 1 H), 4.14 - 4.36 (m, 2 H), 4.07 (t, 1 H), 3.57 (q, 1 H), 2.65 (m, 1H), 2.23(s,3H),1.97-2.34 (m, 4 H), 1.59-1.85 (m,2H), 1.49 (s,3H), 1.39-1.59 (m, 3 H), 0.90 (s, 3 H) 152 101108588 201247697 125 F 51% LC-MS (ESI POS): 551.22 MH+ [a]D25 = + 57.3 (c 0.3, MeOH) •H NMR (300 MHz, DMSO-d6) ppm 8.74 (dd, 1 H), 8.26 (dd, 1 H), 7.93 (d, 1 H), 7.50 (dd, 1H), 7.46(dd, 1H), 7.40 (d,lH), 7.26 (dd, 1 H), 6.28 (dd,1 H),6.07 (s,lH), 5.53 - 5.78 (m,lH), 5.53 (dd,lH), 4.97 (t,lH), 4.58 (dd, 1 H), 4.35 (dd, 1 H), 4.28(t,lH),4.14-4.25(m, 1 H), 3.57 - 3.77 (m, 1 H), 2.72 - 2.85 (m, 1 H), 2.56 -2.70 (m, 1 H), 2.10-2.31 (m, 3 H), 1.54- 1.90 (m, 4 H), 1.50 (s, 3 H), 0.94 (s, 3 H) 126 F 10% LC-MS (ESI POS): 501.14 MH+ [a]D25 = +78.05 (c 0.0925; CHC13) lH NMR (300 MHz, DMSO-d^) ppm 8.29 (dd,1 H),8.21 (dd, 1 H), 7.38 (ddd, l H)} 7.31 (ddd, 1H), 7.26 (dd, 1 H),6.28 (dd, 1 H),6.08 (s,1 H), 5.53-5.74 (m, 1 H), 5.51 (dd, 1 H), 4.95 (t, 1 H), 4.50 (dd, 1 H), 4.30 (dd, 1 H), 4.12 - 4.24 (m, 2 H), 3.53 -3.71 (m,lH), 2.55-2.75 (m, 2 H), 1.98 - 2.33 (m, 3 H), 1.51-1.86 (m,4H)51.49 (s, 3 H), 0.91 (s, 3 H) 101108588 153 201247697 127 F 79% LC-MS (ESI POS): 514.09 MH+ [a]D25 = +70.69 (c 0.26, MeOH) lK NMR (300 MHz, DMSO-de) ppm 7.26 (d, 1 H), 7.15 (t, 1H), 6.58 - 6.95 (m, 3 H), 6.28 (dd, 1 H),6.08 (s,1 H), 5.52 - 5.82 (m, 1 H), 5.50 (d, lH),4.91(t, lH),4,50(dd, 1 H), 4.28 (dd,l H)s4.16- 4.28 (m, 1 H),4.10(t, 1 H), 3.58 (dd, 1 H), 2.54-2.68 (m,2H), 2.27 (s, 3 H), 2.03-2.34 (m, 3 H), 1.62-1.90 (m,2H),1.49(s,3H), 1.37-1.62 (m, 2 H), 0.90 (s, 3 H) 128 5% LC-MS (ESI POS): 518.12 MH+ [a]D25 =+ 37.67 (c0.24, MeOH) lH NMR (300 MHz, DMSO-d6) ppm 7.25 (dd,lH), 7.07 -7.20 (m, 2 H), 6.91 -7.07 (m,2H), 6.28 (dd, IH), 6.08 (s, I H), 5.52 - 5.76 (m, 1 H), 5.51 (<1山 1 H),4.93 (t,lH), 4.49 (dd, 1 H), 4.27 (dd, l H),4.16-4.27 (m,1 H),4.10 (t, 1 H), 3.59 (q, 1 H), 2.54 -2.71 (m,2 H),2.10-133 (m,2 H),1.99 - 2.10 (m,1 H), 1.49 (s, 3 H), 1.42-1.81 (m,4 H),0.90 (s,3 H) 101108588 154 201247697 129 87% LC-MS (ESI POS): 534.1 MH+ [a]D25 = +69.70 (c 0.2 MeOH) !H NMR (300 MHz, DMSO-dg) ppm 7.30 (t, 1 H), 7.26 (dd, 1 H), 6.98 - 7.06 (m, 2 H), 6.93 (ddd, 1 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.55 -5.81 (m, 1 H), 5.52 (dd, 1 H), 4.95 (t, 1 H), 4.47 (dd, 1 H), 4.29 (dd, 1 H)s 4.18-4.25 (m, 1 H), 3.51 - 3.69 (m, 1 H), 2.54 - 2.70 (m, 2 H), 2.02 -2.34(m,3H), 1.62- 1.88 (m,3H),1.51-1.62(m,2 H), 1.49 (s, 3 H), 0.90 (s, 3 H) 130 68% LC-MS (ESI POS): 568.21 MH+ Nd25 = + 49.5 (c 0.2 MeOH) *Η NMR (300 MHz, DMSO-de) ppm 7.53 - 7.74 (m, 2 H), 7.26 (dd, 1 H), 7.03 - 7.20 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.55 - 5.85 (m, 1 H), 5.52 (dd, lH),4.97(t, 1 H), 4.47 (dd,lH), 4.30 (dd, 1 H), 4.16-4.25 (m, 2 H), 3.56 -3.73(m, 1 H), 2.55-2.71 (m, 2 H), 2.04 - 2.30 (m, 3 H), 1.64- 1.86 (m, 2 H), 1.51 -1.64(111,2 H), 1.50 (s, 3 H), 0.92 (s, 3 H) 101108588 155 201247697 131 95% LC-MS (ESI POS): 518.2 MH+ [a]D25 = + 69.15 (c = 0.26, MeOH) *H NMR (300 MHz, DMSO-dg) ppm 7.28 - 7.40 (m, 1 H), 7.26 (dd, 1 H), 6.73 - 6.92 (m, 3 H), 6.28 (dd, I H), 6.08 (s, 1 H), 5.54 - 5.77 (m, 1 H), 5.51(dd, lH),4.94(t, 1H), 4.47 (dds 1 H),4.29(dd, 1 H), 4.18 - 4.24 (m,lH), 4.16 (t, 1 H), 3.51 - 3.66 (m, 1 H), 2.63 (dd, 1 H), 2.55 - 2.70 (m, 1 H), 2.02 - 2.26 (m, 3 H), 1.63 - 1.86 (m, 2 H), 1.51 -1.61 (m, 2 H), 1.49 (s, 3 H), 0,91 (s,3 H) 132 24% LC-MS (ESI POS): 514.23 MH+ [a]D25 = + 54.83 (c 0.24, MeOH) lH NMR (300 MHz, DMSO-de) ppm 7.30 (dd, 1 H),7.28 (dd, 1H), 7.11-7.24 (m, 2 H),7.05(td, 1H), 6.31(dd, 1 H), 6.12 (s,lH), 5.53-5.84 (m, 1 H), 5.50 (dd, 1 H), 4.88 (UH),439(dd, 1 H),4.19 -4.30(m,lH),4.14(dd,l H), 3.85 (t, 1 H), 3.53 - 3.72 (m, 1H), 2.58-2.70 (m,l H), 2.41 (dd, 1 H), 2.23 -2.38 (m, 2 H), 2.15 (s, 3 H), 2.03-2.13(m,lH),1.70-1.84 (m,lH),1.53-1.73 (m, 3 H), 1.51 (s, 3 H), 0.90 (s,3H) 101108588 156 201247697 133 38% LC-MS (ESI POS): 548.21 MH+ [a]D25 = +54.96 (c 0.25, MeOH) 'H NMR (300 MHz, DMSO-d<i) ppm 7.30 (d, 1 H), 7.26 (dd, 1 H), 6.96 (d, 1 H), 6.82 (dd, 1 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.52 - 5.78 (m, 1 H), 5.51 (d, 1 H), 4.93 (U 1 H), 4.49 (dd,〗H), 4.28 (dd, 1H), 4.16 - 4.27 (m, 1H), 4.11 (t,lH), 3.59 (q,lH), 2.54 - 2.69 (m, 2 H), 1.97-2.36 (m, 3 H), 2.29 (s, 3 H), 1.41 - 1.81 (m,4H), 1.49 (s, 3 H), 0.90 (s, 3 H) 134 ψ 36% LC-MS (ESI POS): 602.17 MH+ [a]D25 = + 48.8 (c 0.25, MeOH) lH NMR (300 MHz, DMSO-d6)ppm7.62(d, 1H),7.11-7.40 (m, 3 H), 6.28 (dd, 1 H), 6.08 (s,1 H),5.55 - 5.76 (m, 1 H), 5.53 (dd, 1 H), 4.98 (t, 1 H), 4.46 (dd, 1 H), 4.30 (dd, 1 H), 4.14-4.28 (m, 2 H), 3.52 - 3.72 (m, 1 H), 2.73 (<Η1Η),2.56-2·67(ηι,1 H), 2.01 - 2.34 (m, 3 H), 1.63 -1.87 (m,2 H), 1.51 -1.63 (m,2H),1.49(s,3H),0.9I (s,3H) 101108588 157 201247697 135 鼻 68% LC-MS(ESI POS): 568.18 MH+ [α]〇25 = +53.21 (c 0.28, MeOH) 'H NMR (300 MHz, DMSO-d6) ppm 7.52 (d, 1 H), 7.26 (dd, 1 H), 7.20 (d, 1 H)} 6.98 (dd, 1 H), 6.29 (dd, 1 H), 6.08 (s, 1 H), 5.54 - 5.74 (m, IH), 5.52 (d,lH), 4.96 (t, 1 H), 4.46 (dd, 1H), 4.29 (dd, 1 H), 4.19-4.24 (m, 1 H), 4.18 (t, 1 H), 3.50-3.68 (m, 1 H), 2.65 (dd, 1 H), 2.54-2.61 (m,l H),2.01 -2.31 (m, 3 H), 1.62 - 1.84 (m, 2 H),1.51-1.62 (in,2 H),1.49 (s,3H), 0.90 (s, 3 H) 136 P 52% LC-MS (ESI POS): 578.19 MH+ [a]D25 = + 56.2 (c 0.2, MeOH) *H NMR (300 MHz, DMSO-de) ppm 7.39 - 7.50 (m, 2 H), 7.25 (dd, 1 H), 6.86 - 7.02 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.53 - 5.77 (m, 1 H), 5.51 (dd, 1 H), 4.95 (t, 1 H), 4.47 (dd, 1 H), 4.27 (dd, 1 H), 4.17-4.23 (m,lH), 4.14 (t, 1 H), 3.59 (q, 1 H), 2.54 -2.68 (m,2 H),2.01 -2.25 (m, 3 H), 1.61-1.85 (m, 2 H), 1.50-1.61 (m, 2 H), 1.49 (s,3H),0.90(s,3H) 101108588 158 201247697 137 Γ rrCN 0X^:J P 39% LC-MS (ESI POS): 525.32 MH+ [cc]d25 = + 19.35 (c 0.55, DMF) *H NMR (300 MHz, DMSO-de) ppm 7.59 - 7.86 (m, 2 H), 7.26 (dd, 1 H), 6.99-7.18 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s,1 H),5.54 (dd,1 H), 5.46 -5.75 (m, 1 H), 4.99 (t, 1 H), 4.44 (dd, 1 H), 4.29 (dd, 1 H), 4.24 (t, 1 H), 4.13-4.23 (m, 1 H), 3.55 -3.73 (m, 1 H), 2.77 (dd, 1 H), 2.54 -2.71 (m, 1 H), 2.00-2.25 (m,3H), 1.65- 1.90 (m, 2 H), 1.51 -1.65 (m,2H), 1.49 (s, 3 H), 0.91 (s, 3 H) 138 T NH2 18% LC-MS (ESI POS): 543.35 MH+ [a]D25 = +52.38 (c 0.21, MeOH) lH NMR (300 MHz, DMSO-de) ppm 7.78 - 7.89 (m, 2 H), 7.78 (br. s., 1 H), 7.26 (d, 1 H), 7.15 (br.s., 1 H), 6.89-7.04 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.54 - 5.77 (m, 1H),5.52 (d, lH),4.95(t, 1 H), 4.49 (dd^H), 4.30 (dd, lH),4.13-4.25(m,2H), 3.50 - 3.72 (m, 1 H), 2.57 -2.76 (m, 2 H), 1.98 - 239 (m,3H), 1.64-1.91 (m,2 H), 1.52· 1.64 (m,2 H),1.50 (s, 3 H), 0.91 (s, 3 H) 101108588 159 201247697 LC-MS (ESI POS): 584.26 MH+ [a]D25 = + 63.04 (c 0.25,MeOH) 〇 J; j〇rt 15% lR NMR (300 MHz, DMSO-de) ppm 7.27 (m, 3 H), 7.07 139 (d, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.49 - 5.78 (m, 1 H), 5.52 (dd, 1^4.94(1,1 H), Ψ 4.49 (dd, 1H), 4.28 (dd,l H), 4.11 -4.23(m, 1 H),4.16 (t, 1 H), 3.48 - 3.75 (m, 1 H), 2.56-2.70 (m,2H)s 1.99-2.25 (m, 3 H),1.60· 1.82 (m,2H), 1.49 (s, 3 H), 1.28-1.60 (m,2H), 0.91 (s, 3 H) LC-MS (ESI POS): 594.18 MH+ [α]ϋ25 = + 50.7 (c 0.2 MeOH) τ ^Y°yC lH NMR (300 MHz, DMSO-d^) ppm 7.16 - 7.35 (m, 3 H), ΌέΛ^η^^ 52% 6.93-7.11 (m, 2 H), 6.28 140 Η°Υ^Ρ\..〇ϊ (dd, 1 H), 6.08 (s, 1 H), 5.54 -5.87 (m, lH),5.51(dd,l H),4.94 (t,lH),4.49 (dd, 1 1 H), 4.29 (dd, 1 H), 4.17 -4.23 (m, 1 H), 4.16 (t, 1 H), 3.50 - 3.69 (m,lH)9 3.32 (s, 3H),2.56-2.71 (m,2H), 2.02 - 2.27 (m, 3 H), 1.63 -1.86 (m, 2 H), 1.51-1.63 (m,2H),1.50 (s,3H), 0.91 Cs,3H) 101108588 160 201247697 LC-MS (ESI POS): 582.34 MH+ [c〇d25 = + 64.4 (c 0.2, MeOH) 'H NMR (300 MHz, DMSO- d6) ppm 7.25 (dd, l H),7.06 61% -7.16(m,2H), 6.81-6.93 141 (m, 2 H), 6.28 (dd, 1 H), 6.08 ^jXuy" (s, l H), 5.52 - 5.83 (m, 1 H), Xjzj^ 5.50 (dd, 1 H), 4.90 (t, 1 H), 4.51 (dd, 1 H), 4.27 (dd, 1 H),4.15-4.23(m, 1H),4.07 (t, 1 H), 3.50 - 3.64 (m, 1 H), 2.55-2.71 (m}2H), 2.33-2.45 (m, 1 H), 2.02 - 2.30 (m,3H), 1.51 - 1.88 (m, 8 H), 1.49 (s, 3 H), 1.12-1.44 (m, 6 H), 0.90 (s, 3 H) LC-MS (ESI POS): 582.22 MH+ [a]D25 = + 12.6 (c 0.4, CHC13) JH NMR (300 MH2, DMSO-d6)ppm 7.52 - 7.62 (m, 2 H), 7.46 (dd, 1H), 7.38 (dd, 1 〇J^ Xj 15% H), 7.26 (dd, 1 H)s 7.09 (dd, 142 ΗΟγ^ΐί 7 lH),6.94-7.05(m,2H), 6.28 (dd, 1 H), 6.08 (s, 1 H), XJv^ 5.54 - 5.77 (m, 1 H), 5.52 〇T 丫 F (dd, 1 H), 4.95 (t, 1 H), 4.52 (dd, 1 H), 4.30 (dd, 1 H), 4.20-4.25(m, lH),4.16(t, 1 H), 3.52 - 3.69 (m, 1 H), 2.55 - 2.71 (m, 2 H), 1.99 -2.32 (m, 3 H), 1.62 - L89 (m,2H), 1.52- 1.62 (m, 2 H), 1.50 (s, 3 H), 0.92 (s, 3 H) 101108588 161 201247697 143 30% LC-MS (ESI POS): 558.33 MH+ [a]D25 = + 49.3 (c0.2 MeOH) lH NMR (300 MHz, DMSO-de) ppm 7.73 - 7.96 (m, 2 H), 7.26 (dd, 1 H), 6.93-7.11 (m,2H), 6.28 (dd, 1 H), 6.08 (s, 1H), 5.54-5.81 (m,lH), 5.52 (dd, 1 H), 4.98 (t, 1 H), 4.47 (dd, 1 H), 4.30 (dd, 1 H), 4.17 - 4.26 (m, 2 H), 3.81 (s, 3 H), 3.54 - 3.70 (m, 1 H), 2.55 - 2.85 (m, 2 H), 2.01 - 2.26 (m, 3 H), 1.64-1.87 (m,2H),1.51 -1.64(m,2 H), 1.49 (s, 3 H), 0.92 (s, 3 H) 144 β 50% LC-MS (ESI POS): 578.32 MH+ Ia]〇25 = + 44.0 (c 0.2, MeOH) 'H NMR (300 MHz, DMSO-d6) ppm 7.72 - 7.87 (ra, 2 H), 7.26 (dd, 1 H), 7.06 - 7.19 (m, 2 H), 6.29 (dd, 1 H), 6.08 (s, 1 H), 5.53 (dd, 1 H), 5.46 -5.85 (m, 1 H), 4.91-5.05 (m, 1 H), 4.47 (dd, 1 H), 4.31 (dd, lH),4.26(t,lH), 4.15 -4.24 (m, 1 H), 3.56 - 3.72 (m, 1 H), 3.12 (s, 3 H), 2.77 (dd, 1 H), 2.58 - 2.69 (m, 1 H), 2.02 - 2.32 (m, 3 H), 1.64 -1.86 (m, 2 H), 1.52-1.64 (m,2H), 1.50 (s,3H), 0.92 (s,3H) 101108588 162 201247697 145 F 16% LC-MS (ESI POS): 525.16 MH+ [a]〇25 = +90.32 (c 0.25; DCM) *Η NMR (300 MHz, DMSO-d6) ppm 7.49 (t, 1 H), 7.37 -7.45 (m, 2 H), 7.30 (ddd, 1 H), 7.26 (dd, 1H), 6.28 (dd, 1H), 6.08(s, 1H),5.52-5.74 (m, I H), 5.52 (dd, 1 H), 4.95 (t, 1 H), 4.48 (dd, 1 H), 4.31 (dd, 1 H), 4.20-4.27 (ra, 1 H), 4.21 (t, 1 H), 3.49 -3.71 (m, 1 H), 2.67 (dd, l H), 2.56-2.63 (m, 1H), 1.98-2.27 (m, 3 H)’ 1.63-1.88 (m,2H), 1.51 -1.63 (m, 2 H), 1.50 (s, 3 H), 0.91 (s, 3 H) 146 9» F 25% LC-MS (ESI POS): 579.25 MH+ [a]D25 = +45.41 (c 0.0925; MeOH) lHNMR(300MHz,DMSO-dfi) ppm 7.60 - 7.79 (m, 2 H), 7.26 (dd, 1 H), 7.17 (s, 2 H), 7.01 -7.12 (m, 2 H), 6.29 (dd, 1H), 6.08 (s,lH), 5.52 -5.80 (m,lH), 5.52 (dd,l H),4.47(d,l H), 4.30 (d,l H), 4.21 (t,lH), 4.12-4.23 (m, 1 H), 3.56-3.71 (m, 1 H), 2.67-2.78 (m,1 H), 2.55 -2.67 (m, 1 H), 2.01 - 2.33 (m, 3 H), 1.63-1.87 (m,2 H), 1.51-1.63 (m, 2 H), 1.50 (st 3 H), 0.92 (s, 3 H) 101108588 163 201247697 147 68% LC-MS (ESI POS): 540.28 MH+ [α]〇25 = + 78.53 (c 0.3; MeOH) !H NMR (300 MHz, DMSO-d6) ppm 7.25 (dd, 1 H), 6.94 -7.07(m,2H), 6.76-6.93 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.52 - 5.79 (m, 1 H), 5.50 (d, 1 H), 4.90 (t, 1 H), 4.50 (dd, 1 H), 4.27 (dd, 1 H), 4.14-4.21 (m, 1 H),4.06 (t, 1 H), 3.44 - 3.68 (m, 1 H), 2.53-2.70 (m,2H), 1.97-2.30 (m,3 H), 1.79- 1.92 (m,1 H),1.60 - L79 (m,2 H),1.51 -1.60 (m,1 H),1.49 (s,3H), 1.42- 1.49 (m,lH), 0.90 (s, 3 H), 0.78 - 0.88 (m, 2H),0.50-0.65(m,2H) 148 41% LC-MS (ESI POS): 556.38 MH+ [α]〇2ί = +71.25 (c 0.4, MeOH) *H NMR (300 MHz, DMSO-d6)ppm 7.27 - 7.33 (m, 2 H), 7.26 (d,lH), 6.78-6.98 (m, 2H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.53 - 5.75 (m, 1 H), 5.51 (dd, 1 H), 4.90 (t, 1 H), 4.51 (dd, 1 H), 4.28 (dd, 1 H), 4.16 - 4.23 (m, 1 H), 4.08 (t, 1 H), 3.49 - 3.69 (m, 1 H), 2.55-2.70 (111,2^1.98-2.32 (m, 3 H), 1.61 -1.84 (m,2H), 1.52-1.61 (m, 1 H), 1.49 (s, 3 H), 1.40-1.48 (m, 1 H), 1.24 (s, 9 H), 0.90 (s,3H) 101108588 164 201247697 149 17% LC-MS (ESI POS): 543.24 MH+ [a]D25 = +32.5 (c 0.0415; MeOH) 'H NMR (300 MHz, DMSO-d^) ppm 10.04 (s, 1 H), 8.20 (d, 1 H), 7.50 (d, 2 H), 7.26 (d, 1 H), 6.78 - 7.02 (m, 2 HX6.28(dd, 1H), 6.08 (s, 1 H), 5.51 -5.79 (m, 1 H), 5.50 (d, 1 H), 4.92 (t, I H), 4.51 (dd, 1H), 4.27(dd,lH), 4.15 - 4.26 (m, 1 H), 4.07 (t, 1 H), 3.44 - 3.67 (m, 1 H), 2.60-2.71 (m,2H), L.96-2.32 (m,3 H),1.60- 1.81 (m,2H), 1.41 - 1.58 (m, 2 H), 1.49 (s,3H), 0.90 (ss 3 H) ISO 1 34% LC-MS (ESIPOS): 568.23 MH+ [a]D25 = + 57.8 (c0.2, MeOH) lH NMR (300 MHz, DMSO-de) ppm 7.43 - 7.64 (m, 1 H), 7.12 - 7.39 (m, 4 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.44 -5.79 (m, 1 H), 5.53 (d, 1 H), 4.96 (t, 1 H), 4.48 (dd, 1 H),4.31 (dd, 1 H), 4.15-4.31 (m, 2 H), 3.62 (q, 1 H), 2.55 - 2.79 (m, 3 H), 1.96-2.25 (ms 2 H), 1.63-1.93 (m, 2 H), 1.50 (s, 3 H), 1.27 -1.63 (m, 2 H), 0.92 (s, 3 H) 101108588 165 201247697 151 P 15% LC-MS (ESI POS): 584.2 MH+ [a】D2S = +76.6 (c 0.22, DCM) !H NMR (300 MHz, DMSO-(^) ppm 7.41 (t, 1 H), 7.26 (dd, 1 H), 6.90 - 7.02 (m, 3 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.50 - 5.77 (m, 1 H), 5.50 -5.54 (m, 1H), 4.92-4.98 (m, 1 H)} 4.46 (dd, 1 H), 4.29 (dd, 1 H), 4.20 (t, 1 H), 4.07 -4.24 (m,1 H),3.61 (q, 1 H), 2.67 (dd, 2 H), 2.04 -2.28 (m, 3 H), 1.65 - 1.82 (m, 2 H), 1.50 (s, 3 H), 1.55 (dd,2H), 0.91 (s,3H) 152 F 71% LC-MS (ESI POS): 578.04 MH+ [a]〇2S = + 65.8 (c 0.0900, MeOH) *H NMR (300 MHz, DMSO-de) ppm 7.19 - 7.33 (m,2 H), 7.10 - 7.19 (m, 2 H), 6.97 (ddd, 1 Η), 6.2B (dd, 1 H), 6.08 (s, 1 H), 5.53 - 5.78 (m, 1 H), 5.52 (dd, 1 H), 4.95 (t, 1 H), 4.46 (dd, 1 H), 4.29 (dd, 1 H), 4.18-4.26 (m, 1 H), 4.17 (t, 1 H), 3.47 - 3.75 (m, 1 H), 2.63 (dd, 1 H), 2.55 -2.70 (m,lH),1.98-2.37 (m, 3 H), 1.60 - 1.88 (m, 2 H),l_51 -1.60(m,2H),l_49 (s, 3 H), 0.90 (s, 3 H) 101108588 166 201247697 LC-MS (ESI POS): 557.1 MH+ 乂 [a]D25 = +71.16(c 0.6, MeOH) lU NMR (300 MHz, DMSO- % 0 r r〇 de) ppm 9.21 (s, 1 H), 7.98 (d,lH),7.75(d, 1H), 7.26 (dd, 1 H), 7.21 (dd, 1 H), 153 46% 6.28 (dd, 1 H), 6.07 (s3 1 H), 5.54 - 5.77 (m, 1 H), 5.52 P (dd, 1 H), 4.95 (t, 1 H), 4.55 (dd,lH),4.33 (dd, 1 H), 4.20 - 4.27 (m, 1 H), 4.22 (t, 1 H), 3.51 -3.79 (m, 1 H), 2.69 (dd, 1 H), 2.54 - 2.65 (m, 1 H), 2.02-2.31 (m, 3 H), 1.64- 1.89 (m, 2 H), L52 -1.63 (m}2H), 1.50 (s, 3 H), 0.92 (s, 3 H) LC-MS (ESI POS): 647.97 MH+ [a]D25 = + 56.0 (c 0.24, MeOH) T f*<^v0''s〇2CF» νΗ NMR (300 MHz, DMSO-d^) ppm 7.31 > 7.52 (m, 2 H), 7.26 (dd, 1 H), 6.95-7.18 154 磨.’,、 82% (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.44 - 5.77 (m, 1 H), 5.52 (dd, 1 H), 4.95 (t, 1 H), 4.48 (dd, 1 H), 4.29 (dd, 1 H), 4.11-4.24 (m, 1H), 4.18 (t, 1 H), 3.62 (q, 1 H), 2.55 -2.72 (m, 2 H), 1.98-2.30 (m,3H), 1.44 - 1.83 (m, 4 * H), 1.49 (s, 3 H), 0.91 (s, 3 H) 101108588 167 201247697 155 19% LC-MS (ESIPOS): 540.1 MH+ [«]d2S = + 43.6 (c0.3; MeOH) *H NMR (300 MHz, DMSO-d6) ppm 7.26 (dd, 1 H), 7.14 (t, 1 H), 6.75 (ddd, 1 H), 6.55 -6.70 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.54 - 5.79 (m, 1 H), 5.51 (dd, 1 H), 4.91 (t, 1 H), 4.50 (dd, 1 H), 4.28 (dds 1 H), 4.17-4.23 (m91 H), 4.11 (t,lH), 3.49-3.66 (m, 1 H), 2.60-2.69 (m, 1 H), 2.56 (dd, 1 H), 2.00 -2.25 (m, 3 H), 1.88 (tt, 1 H), 1.61 -1.81 (m,2H), 1.51 -1.59 (m,2H), 1.50 (s, 3 H), 0.91 -0.97 (m, 2 H), 0.90 (s, 3H), 0.49-0.71 (m,2H) 156 21% LC-MS (ESI POS): 597.16 MH+ [〇t]D25 = +54.6 (c 0.29. MeOH) !H NMR (300 MHz, DMSO-d$) ppm 7.26 (d, 1 H), 7.05 (m, 2 H), 6.88 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.37 -5.82 (m, 1 H), 5.51 (br. s., 1 H), 4.74 - 5.03 (m, 1 H), 4.51 (dd, 1 H), 4.21 (m, 1 H), 4.27 (dd,1 H), 4.07 (t, 1 H),3.57 (q, 1 H), 2.77 - 2.98 (ra, 2 H),2.56 - 2.70 (m,2 H),2.13 -2.43 (m,7 H), 2.03 -2.12 (m,lH),1.59_1.87(m,2 H), 1.38 - 1.59 (m, 5 H), 1.49 (s, 3 H), 0.80 - 1.08 (m, 2 H), 0.90 (s, 3 H) 101108588 168 201247697 [實施例16]
THF/水 開放空氣
(4&8,仆11,53,6&8,6匕11,9&8,1(^8,1(^8,128)-仆,12-二氟_5_經 基 -4a,6a- 二曱基 -2-側氧基 -8- 苯基 -2,4a,4b,5,6,6aJ8}9,9a,10,10aJ10bJll512--f- izg A-7-»f-8-πγ 搭烯并[2,l-a]菲-6b-羧酸(化合物158)之製備 於157 (733毫克’ 1.461毫莫耳)於四氫呋喃(12毫升)之溶液 内於0°C通入空氣15分鐘;然後徐緩添加6N氫氧化鈉(〇 974 毫升’ 5.85毫莫耳)及又於0°C通入空氣5分鐘。任反應混合 物溫熱至室溫及於室溫擾拌隔夜。反應混合物酸化至pH 1 及蒸發去除四氫呋喃。水層以乙酸乙酯(1〇〇毫升χ3)萃取。 組合有機萃取物以鹽水洗滌,脫水(硫酸鈉)及濃縮❶粗產物 於DCM/AcOEt/HC02H 39.5:0.5:50藉二氧化石夕凝膠急速層析 術純化’獲得396毫克標題化合物(56%) 〇 LC-MS (ESI POS): 486.1 (MH+) 表8化合物係如先前對化合物58 158所述製備。 101108588 169 201247697 [表8] 化合物 結構式 產率 分析 159 90% LC MS (ESI POS): 519:9 (MH+) 160 60% LC MS (ESI POS): 52〇T〇 (MH+) 161 X F 53% LC MS (ESI POS): 500.1 (MH+) 162 F 97% LC MS (ESI POS): 500.1 (MH+) 163 f 16% LC MS (ESI POS): 500.2 (MH+) 164 Ρ 84% LC MS (ESI POS): 520.0 (MH+) 165 Ρ 93% LC MS (ESI POS): 504.1 (MH+) 166 1 呈粗產物 使用 LC MS (ESI POS): 487.0 (MH+) 101108588 170 201247697 167 93% LC MS (ESI POS): 504.1 (MH+) 168 Ψ 46% LC MS (ESI POS): 534.1 (MH+) [實施例17]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5·· 基 -4a,6a- 二曱基 -2- 側氧基 -8- 苯基 -2,4&,41),5,6,63,8,9,9&,10,10&,1013,11,12-十四氫_7-<»等-8_吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯(化合物169)之製 備 化合物158 (396毫克,0.816毫莫耳)、HATU (341毫克, 0.897毫莫耳)及N-曱基咮啉(90微升,0.816毫莫耳)於無水 DMF (5毫升)之混合物於70°C於氮氣環境下攪拌4小時及 LC-MS顯示期望之活性酯生成。溶液冷卻至室溫及添加無水 硫化氫鈉(137毫克,2.447毫莫耳)。混合物於室溫攪拌25分 鐘,然後添加溴氟曱烧(1.223毫升,2.447毫莫耳)於DMF之2 Μ溶液及混合物於室溫攪拌2小時隔夜。 加水(20毫升)至反應混合物及所形成之沈澱經過滤。收集 101108588 171 201247697 之沈殿於AcOEt/DCM 5:95至AcOEt/DCM 10:90之梯度洗 k,於一氧化發凝膠上藉急速層析術純化及然後藉製備性 HPLC純化獲得39毫克標題化合物(9%產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.27 - 7.36 (m, 2 Η), 7.24 (dd, 1 Η), 6.93 - 7.09 (m, 3 Η), 6.28 (dd, 1 Η), 6.08 (s, 1 Η), 5.92 (dd, 1 Η), 5.84 (dd, 1 Η), 5.56 (dd, 1 Η), 5.47 - 5.74 (m, 1 Η), 4.22 (t, 1 Η), 4.14 - 4.23 (m, 1 Η), 3.59 (q, 1 Η), 2.64 (dd, l H), 2.54 - 2.71 (m> 1 H), 2.07 - 2.33 (m, 2 H), 1.94 - 2.07 (m, 1 H), 1.84 (d, 1 H), 1.68 - 1.80 (m, 1 H), 1.52 - 1.66 (m, 2 H), 1.50 (s,3H), 0.98 (s, 3 H) LC-MS (ESI POS): 534.17 (MH+) [al〇25 = + 87.4 (c 0.114; CHC13) 表9之化合物係如先前對化合物169所述,始於適當酸衍生 物製備: [表9] 化合物 結構式 產率 分析 170 42% LC-MS (ESI POS): 568.09 MH+ [α]〇25 = +55.80 (c 0.157; CHClj) Ή NMR (300 MHz, DMSO-de) ppm 7.29 -7.43 (m, 2 H), 7.24 (dd, 1 H), 6.89-7.11(m,2H), 6.28 (dd, 1 H), 6.09 (s, 1 H), 5.92 (dd, 1 H), 5.84 (dd, 1H), 5.54-5.62 (m, 1 H), 5.47-5.74 (χη,ΙΗ), 4.04 - 4.34 (m, 2 H), 3.50-3.68 (m,lH), 2.65 (t, 2 H), 2.05-2.31 (m,2 H), 1.92-2.05 (m, 1H), 1.68 -1.89 (m, 2 H), 1.52 - 1.66 (m, 2 H), 1.49 (s, 3 H), 0.98 (s, 3 H) 172 101108588 201247697 171 50% LC-MS (ESI POS): 548.23 MH+ [α]〇25 = + 64.0 (c 0.24, CHC13) ^NMRiSOO MHz, DMSO-dc) ppm 7.24 (dd, 1 H), 7.17 (t, 1 H),6.74-6.89 (m, 3 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.92 (dd, 1 H), 5.84 (dd, 1 H), 5.56 (dd, 1 H), 5.46-5.74 (m, 1 H), 4.17-4.29 (m, 1 H), 4.19 (t, 1 H), 3.58 (q, 1 H), 2.55 - 2.67 (m,2 H), 2.27 (s,3H), 1.95-2.25 (m, 3 H), 1.83 (d, 1H), 1.68-1.79 (m, 1 H), 1.52-1.66 (m,2H), 1.49 (s, 3 H), 0.98 (s, 3 H) 172 37% LC-MS (ESI POS): 547.91 MH+ [a]D2S = + 77.1 (c0.2 dmso) 'HNMR(300 MHz, DMSO-dfi) ppm 7.35 (dd, 1 H),7.27(dd, 1 H), 7.17-7.24 (m, 1 H), 7.12-7.17 (m, 1 H), 7.07 (td, 1 H), 6.31 (dd, 1 H), 6.09-6.19 (m, 1 H), 5.90 (dd, 1 H), 5.81 (dd, 1 H), 5.57-5.79 (m, 1 H), 5.56 (dd, 1 H), 4.15-4.35 (m, 1H),3.92 (t, 1 H), 3.54-3.66 (m, 1 H), 2.22-2.47 (m,4H), 2.16 (s, 3 H), 1.95-2.10 (m, 1H), 1.55-1.87(m,4 H), 1.51(s,3H), 0.98 (s, 3 H)_ 173 101108588 201247697 173 〇JFj〇r a 14% LC-MS (ESI POS): 548.11 MH+ [a]D25 = + 66.4 (c 0.103, CHCb) 'HNMR (300 MHz, DMSO-d6) ppm 7.24 (dd, 1 H), 7.04 - 7.16 (m, 2 H), 6.82 - 7.02 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.92 (dd, 1 H), 5.84 (dd, 1 H), 5.55 (dd, 1 H), 5.49 -5.73 (ra, 1 H), 4.17-4.29 (m, 1 H),4.16(t, 1 H), 3.58 (q, 1 H), 2.62-2.79 (m, 1H), 2.53 - 2.62 (m, l H), 2.23 (s,3H), 1.93-2.22 (m,3H), 1.67-1.88 (m,2H), 1.50- 1.66 (m, 2 H), 1.49 (s, 3 H), 0.97 (s, 3 H) 174 P 29% LC-MS (ESI POS): 568.07 MH+ [a]D25 = + 55.0 (c 0.2, CHClj) 'HNMR (300 MHz, DMSO-d6) ppm 7.33 (t, 1 H), 7.24 (dd, 1 H), 7.01 -7.09 (m, 2 H), 6.97 (ddd, 1 H), 6.28 (dd, 1 H), 6.07 -6.12 (m, 1 H), 5.92 (dd, 1 H), 5.85 (dd, 1 H), 5.57 (dd, 1 H), 5.48 - 5.72 (m, 1 H),4.27(t, 1 H),4.14-4.25 (m, 1 H), 3.48 - 3.68 (m, 1 H), 2.56-2.71 (m, 2 H), 1.94 - 2.24 (m, 4 H), 1.52 - 1.93 (m, 3 H), 1.49 (s, 3 H), 0.98 (s, 3 H) 174 101108588 201247697 175 24% LC-MS (ESI POS): 552.15 MH+ [a]D25 = +76.56 (c 0.25, MeOH) *HNMR (300 MHz, DMSO-de) ppm 7.24 (dd, 1 H), 7.10-7.20 (ra,2H), 7.00-7.10(ηι, 2 H), 6.28 (dd, 1 H), 6.08 (s, t H), 5.93 (dd, 1 H), 5.85 (dd, 1 H), 5.56 (dd, 1 H), 5.41 -5.73 (m, 1 H), 4.11-4.31 (m, 2 H), 3.52-3.69 (m, 1 H), 2.57 - 2.72 (m, 2 H), 2.06-2.34 (m,2H), 1.93-2.05 (m, 1 H), 1.67-1.89 (m,2H), 1.52 - 1.67 (m, 2 H), 1.49 (s, 3 H), 0.98 (s, 3 H) 176 12% LC-MS (ESIPOS): 535.1 MH+ [a]D25 = +29.84(c 0.0925; MeOH) lHNMR(300MHz, DMSO-dfi) ppm 8.33 (d, 1 H), 8.24 (dd, 1 H), 7.42 (ddd, 1 H), 7.35 (dd, 1 H), 7.24 (dd, 1 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.93 (dd, 1 H), 5.85 (dd, 1 H), 5.55 -5.60 (m, 1 H), 5.47 - 5.75 (m, 1 H), 4.30 (t, 1 H), 4.10-4.25 (m, 1 H), 3.55-3.71 (m, 1 H), 2.66 - 2.78 (m, 1 H), 2.59 - 2.66 (m, 1 H), 2.02 - 2.35 (m, 3 H), 1.52- 1.90 (m, 4 H), 1.50 (s, 3 H), 0.99 fs, 3 H) 175 101108588 201247697 177 24% LC-MS (ESIPOS): 552.11 ΜΗ+ [a]D25 = +68.31 (c 0.26, DCM) 'Η NMR (300 MHz, DMSO-d6) ppm 7.29 - 7.49 (m, 1 H), 7.24 (dd, 1 H), 6.69 - 6.91 (m, 3 H), 6.28 (dd, 1 H), 6.09 (s, 1 H), 5.92 (dd, 1 H), 5.85 (dd, 1 H), 5.57 (dd, 1 H), 5.49 -5.74 (m, 1 H), 4.25 (t, 1 H),4.14 - 4.22 (m,1 H), 3.50 - 3.67 (m, 1 H), 2.57 -2.81 (m,2H), 2.07-2.34 (m,2H), 1.95 -2.07 (m,] H), 1.68- 1.92 (m, 2 H), 1.53- 1.68 (m,2H), 1.50 (s, 3 H), 0.98 (s, 3 H) 178 Ρ 35% LC-MS (ESI POS): 602.21 MH+ [a]D25 = + 42.6 (c 0.2, MeOH) 'HNMR (300 MHz, DMSO-de) ppm 7.53 - 7.84 (m, 2 H), 7.24 (dd, 1 H), 7.08-7.21 (m,2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.92 (dd, 1 H), 5.85 (dd, 1 H), 5.58 (dd, 1 H), 5.42 -5.74 (m, 1 H), 4.35 (t, 1 H), 4.07 - 4.29 (m, 1 H), 3.50 - 3.76 (m, 1 H), 2.59 -2.86 (m, 2 H), 1.96-2.35 (111,3¾ 1.69- 1.94 (m, 2 H), 1.53- 1.69 (m, 2 H), 1.50 (s, 3 H), 1.00 (s,3 H) [實施例18] 101108588
106 179 176 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -6b-(2-氟-乙醯基)-5-羥基-4a,6a-二甲基-8-苯基 -4牡,41),5,6,63,613,8,9,9&,10,10&,101),11,12-十四氫-7_崎-8-口丫_ 戊搭烯并P,l-a]菲-2-酮(化合物179)之製備 106(150毫克’ 0.394毫莫耳)、N-苯基羥基胺(86毫克,〇.789 毫莫耳)及三聚曱搭(71.0毫克’ 2.366毫莫耳)於乙醇(13毫升) 之混合物於100°C攪拌20小時。又添加N-苯基羥基胺(47.3毫 克,0.434毫莫耳)及三聚曱醛(52.1毫克,1.735毫莫耳)及混 合物於100°C加熱3小時。溶劑經蒸發及殘餘物於 AcOEt/MeOH/DCM 4.8:0.2:95之梯度洗提,藉二氧化矽凝膠 急速層析術純化獲得144毫克期望化合物(Rf=〇 22於 AcOEt/MeOH/DCM 9.8:0.2:90)。化合物又更於 Dcm 至 DCM/AcOEt87:13梯度洗提,藉二氧化矽凝膠急速層析術純 化獲得122毫克標題化合物(62%產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.27 - 7.34 (m, 2 Η), 7.27 (dd, 1 Η) 6.93 - 7.07 (m, 3 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.52 (d, 1 H), 5.49 - 5.74 (m [ H), 5.37 (dd, 1 H), 5.30 (dd, 1 H), 4.17 - 4.27 (m, 1 H), 4.19 (t, 1 H), 3.56 (q, 1 ^ 2.60 - 2.71 (m,1 H),2.59 (dd,1 H),2.11 - 2.32 (m,2 H), 2.07 (ddd, 1 H),u〇 (d’ 1 H), 1.63 - 1.77 (m, 1 H), 1.51 -1.62 (m, 2 H), 1.50 (s, 3 H), 0.95 (s, 3 H) ’ LC-MS (ESI POS): 502.15 MH+ [a]D25 = + 68.72 (c 0.094; CHC13) 表10列舉之化合物係如先前對化合物179所述藉中間產物 106與適當羥基胺或羥基胺鹽酸鹽之環化加成製備。 101108588 177 201247697 [表 10] 化合物 結構式 產率 分析 180 65% LC-MS (ESI POS): 536.07 MH+ [a]D2S =+50.85 (c 0.0885; CHC13) WNMR (300 MHz, DMSO-d6) ppm 7.30-7.43 (ra,2H), 7.26(dd, 1H), 6.93 - 7.08 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.52 (d, 1 H), 5.47-5.80 (m, 1 H), 5.36 (dd, 1 H), 5.29 (dd, 1H), 4.14-4.25 (m, 1 H), 4.19 (t# 1 H), 3.44 -3.65 (m, 1 H), 2.58 - 2.73 (m, 1 H), 2.60 (dd, 1 H), 1.97-2.30 (m, 3 H), 1.63-1.87 (m,2 H), 1.51 -1.61 (m,2H),1.49(s,3H),0.94 (s,3H) [實施例20]
曱烷磺酸2-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣苯基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\415,5,6,6&,8,9,93,10,1〇3,1013,11,12-十四氫-7-4崎-8-吖-戊搭烯并[2,1-a]菲-6b-基]-2-側氧基-乙基酯(化合物181)之 製備 曱烧磺醯氣(79微升,1.011毫莫耳)於〇〇c於氮氣環境下添 加至123 (450毫克,0.843毫莫耳)及DIPEA (221微升,1.264 178 101108588 201247697 毫莫耳)於DCM (以氣化鈣脫水,20毫扑)之溶液内。混合物 於室溫攪拌2小時。 混合物以DCM稀釋及以2,5%水性碳酸氫鈉洗滌。水相以 乂 萃取,及組合有機相以鹽水洗務,以硫酸納脫水及過 t 濾。溶劑經蒸發去除。 LC-MS (ESI POS):612.2 (MH+) (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-(2-氯-乙醯 基)-8·(4-氣-苯基)-4b,12-二氟-5-羥基-4a,6a-二甲基 -4巳,41),5,6,63,61),8,9,93,1〇,1〇&,1〇1),11,12-十四氫-7-»等-8-吖-戊搭稀并[2,1-a]菲-2-酮(化合物182)之製備 化合物181 (195毫克,〇.319毫莫耳)及氣化鋰(162毫克, 3.82毫莫耳)於無水DMF (6毫升)之混合物於氮氣環境下於 70°C攪拌2小時。 混合物分溶於乙酸乙酯及鹽水’及然後水相以乙酸乙酯萃 取。組合有機相以鹽水洗滌,以硫酸鈉脫水及過濾。溶劑經 蒸發及粗產物藉二氧化矽凝膠急速層析術純化(洗提劑: DCM:MeOH99:l)。獲得固體,以Et20/Et0H(95:5)濕磨獲得 標題化合物(33%產率)。 ’ Ή NMR (300 MHz, DMSO,d6) ppm 7.3〇 - 7.41 (m, 2 H), 7.27 (dd, 1 H), 6.95 - 7.12 (m, 2 H),6.29 (dd,1 H), 6.08 (s,1 H),5.33 - 5.80 (m, 1 H), 5.52 (d,1 H),4.70 (s,2 H),3.96 - 4.33 (m,2 H), 3.60 (q,1 h),2.55 - 2.70 (m, 2 H),2.00 · 2.36 (m,3 HU.83 (d,i h), 1.63 · l·78 (m,1 H),1.28 - 1.63 (m, 2 H), 1.49 (s,3H), 0.92 (s, 3 H) 101108588 179 201247697 LC-MS (ESI POS): 552.21 (MH+) [a]D25 = + 81.85 (c 0.26, CHC13) [實施例21]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-41>,12-二氟-5-羥基-4\6&-二曱基-61)-(2-曱基硫烷基-乙 醯基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-+w&-7-4 -8-吖-戊搭烯并[2,l-a]菲-2-酮(化合物183)之製備 化合物181 (175毫克,0.286毫莫耳)及曱烷硫醇酸鈉(24.05 毫克’ 0.343毫莫耳)於無水DMF (4毫升)之混合物於室溫於 氮氣環境下攪拌3小時。混合物分溶於乙酸乙酯及鹽水,及 水相以乙酸乙酯萃取。組合有機相以鹽水洗滌,以硫酸鈉脫 水及過濾。溶劑經蒸發及殘餘物以乙腈濕磨。所得粗產物藉 二氧化石夕凝膠急速層析術純化(DCM:MeOH 99:1)及然後以 乙醚濕磨獲得期望化合物(16%產率)。 101108588 180 201247697 'H NMR (300 MHz, DMSO-d6) ppm 7.29 - 7.48 (m, 2 H), 7.26 (dd, { H) 6.89 - 7.10 (m, 2 H), 6.29 (dd, 1 H), 6.08 (s, 1 H), 5.53 - 5.78 (m, 1 H), 5.S1 (dd { H), 4.17 - 4.30 (m, 1 H), 4.13 (t, 1 H), 3.70 (d, 1 H), 3.62 (d, 1 H), 3.54 - 3^3 (m 1 H), 2.61 (dd, 1 H), 2.55 > 2.71 (m, 1 H), 2.06 - 2.25 (m, 3 H), 2.04 (s, 3 H)s 1 88 (d, 1 H), 1.63 -1.81 (m, 1 H), 1.51 -1.62 (m, 2 H), 1.50 (s, 3 H), 0.93 (s, 3 fi) LC-MS (ESI POS): 564.24 (MH+) [a]D25 = + 85.92 (c 0.24, CHC13) [實施例22]
(4aS,4bR,5S,6aS,6bR,9aSs10aS,10bS,12S)-8-(4-氣 _ 笨 基)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧美 •2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+raA-7-t^_8_^_;^ 搭婦并[2,1-a]菲-6b-叛酸氯甲基硫醋(化合物184)之製備 化合物159於氮氣環境下溶解於DMF (4毫升);添加碳酸 卸(106毫克,0.769毫莫耳)及溴氯甲烷毫升,i阳毫 莫耳)及混合物於室溫攪拌4小時。反應混合物分溶於水及乙 酸乙酯。有機相經分離及溶劑經去除。粗產物藉二氧化矽凝 膠急速層析術純化(洗提劑DCM/AcOEt 95/5至9/1)與得固 體,固體進一步於乙醚濕磨獲得標題化合物(23%產率)。 181 101108588 201247697 'H NMR (300 MHz, DMSO-d6) ppm 7.28 - 7.35 (m, 2 H), 7.25 (dd, 1 H), 6.83 - 7.04 (m, 2 H), 6.29 (dd, 1 H), 6.09 (s, 1 H), 5.95 (d, 1 H), 5.93 (d, 1 H), 5.61 (dd, 1 H), 5.47 - 5.78 (m, 1 H), 4.20 - 4.35 (m, 1 H), 4.16 (t, 1 H), 3.63 - 3.81 (m, 1 H), 2.77 (dd} 1 H), 2.61 - 2.72 (m, 1 H), 1.96 - 2.26 (m, 3 H), 1.68 - 1.93 (m, 2 H), 1.52 - 1.62 (m, 2 H), 1.50 (s, 3 H), 1.02 (s, 3 H) LC-MS (ESI POS): 568.17 (MH+) [a]D25 = + 56.2 (c 0.3, MeOH) 表11之化合物係如先前對化合物184所述,始於酸159、適 當烷化劑及鹼諸如碳酸鈉、碳酸鉀或三乙基胺與適當溶劑而 製備。 [表 11] 182 101108588 201247697 化合物 結構式 產率 分析 185 33% LC-MS (ESIPOS): 574.3 MH+ Md25 = + 59.5 (c 0.2, MeOH) *H NMR (300 MHz, DMSO-¢^) ppm 7.26 - 7.33 (m, 2 H), 7.26 (dd, 1H),6.89-7,01 (m, 2H),6.29(dd,lH),6.09(s,l H), 5.55 (d,lH), 5.48-5.77 (m, 1H), 4.16-4.34 (m,lH), 4.1 l(t,lH), 3.95 (dd,lH), 3.87 (dd,lH), 3.60-3.75 (m, 1 H), 2.81 (dd,lH), 2.55-2.71 (m, 1 H), 1.95 - 2.31 (m, 3 H), 1.82-1.94 (m,lH), 1.66 -1.82 (m,lH), 1.52-1.61(m, 2 H), 1.50 (s, 3 H), 1.04-1.22 (m, 1 H), 1.00 (s, 3 H), 0.43 -0.60(111,211),0.20-0.37(1^ 2H) 186 25% LC-MS (ESI POS): 559.14 MH+ [a]D25 = +78.96(c 0.25, DCM) ]H NMR (300 MHz, DMSO-de) ppm 7.28 - 7.36 (m, 2 H), 7.26 (dd, 1H), 6.87 - 7.03 (m, 2H), 6.29(dd,lH), 6.09 (s,l H), 5.61 (dd,lH), 5.43-5.78 (m, 1H), 5.11 (d,lH), 5.05 (d, 1H), 4.19-4.38 (m,lH), 4.18 (t,lH), 3.66-3.81 (m,l H),2.78(dd,lH), 2.56-2.70 (111,111),1.96-2.26(111,311), 1.66- 1.88(m,2H),1.52-1.64(m,2H),1.50(s,3H), 1.01 (s, 3 H) 183 101108588 201247697 187 dNxrc, P 24% LC-MS (ESI POS): 577.13 MH+ [a]D25 = +51.0 (c 0.22, MeOH) ]H NMR (300 MHz, DMSO-d«) ppm 7.25 - 7.40 (m, 2 H), 7.23-7.29 (m, 1 H),7.14-7.23 (m, 2 H), 6.85 - 7.07 (m, 2 H), 6.29 (dd, 1 H), 6.09 (s, 1 H), 5.47 - 5.80 (m, 1 H), 5.56 (d, 1 H), 4.46 (s, 2 H), 4.16-4.26 (m, 1 H), 4.11 (t, 1 H), 3.60 - 3.82 (m, 1 H), 2.82 (dd, 1 H), 2.56 - 2.69 (m, 1H), 1.86-2.25 (m, 4 H), 1.65- 1.86 (m, 1 H), 1.50 (s, 3 H), 1.33 - 1.63 (m, 2 H), 1.06 (s, 3 H) 188 20% LC-MS (ESI POS): 602.26 MH+ [a]D25 = + 57.6(c 0.3, MeOH) 'H NMR (300 MHz, DMSO-d6) ppm 7.29 - 7.37 (m, 2 H), 7.26 (dd, 1 H), 6.90 - 7.03 (m, 2 H), 6.29 (dd, 1 H), 6.09 (s, 1 H), 5.64 (d, 1 H), 5.46 -5.81 (m, 1 H), 4.71 - 4.96 (m, 2H), 4.18-4.26(m, 1 H), 4.16 (t, 1 H), 3.50-3.81 (m, 1 H), 2.79 (dd, 1 H), 2.59 -2.68 (m, 1 H), 1.94 - 2.25 (m, 3 H), 1.66- 1.85 (m, 2 H), L.52- 1.63(m,2H), 1.50 (s, 3 H), 1.00 Cs,3H) 184 101108588 201247697 LC-MS (ESI POS): 566.18 MH+ [α]〇25 = + 55 (c 0.21, MeOH) *H NMR (300 MHz, DMSO- 〇xrxc, d^) ppm 7.19 - 7.37 (m, 3 H), 6.86 - 7.04 (m, 2 H), 6.29 189 38% (dd, 1 H), 6.09 (s, 1 H), 5.56 rmP (dd, 1 H), 5.43 - 5.81 (m, 1 H), 4.63 (dt, 2 H), 4.02 - 4.49 (m, 4 H), 3.55 - 3.76 (m, 1 H), 2.82 (dd, 1 H), 2.55 - 2.68 (m, I H), 1.96-2.35 (m, 3 H),1.86(d,lH), 1.68-1.81 (m, 1H), 1.51-1.64(m,2 H), 1.50 (s, 3 H), 0.99 (s, 3 H) [實施例23]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯 _ 苯 基)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7“号-8-口丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氰基曱基g旨(化合物19〇)之 製備 化合物159 (218毫克,0.419毫莫耳)於氮氣環境下溶解於 DMF(5毫升);添加HATU(175毫克,0.461毫莫耳)及‘曱基 咪1#(50.9¾克,0.503毫莫耳)及混合物於室溫搜拌1小時。 然後添加硫化氫鈉(47.0毫克,0.839毫莫耳)及混合物轉成深 綠色。所得混合物於室溫攪拌丨小時,添加2_溴乙腈(OH? 101108588 185 201247697 毫升,1.677毫莫耳)及溶液於室溫於密封容器内攪拌隔夜β 反應混合物以乙S文乙g旨稀釋及有機層以水及鹽水洗條,脫水 (硫酸鈉)及濃縮。粗產物藉二氧化矽凝膠急速層析術純化(洗 提劑DCM/AcOEt95/5至9/1)獲得固體,固體進一步使用乙醚 濕磨獲得期望化合物(22%產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.32 - 7.45 (m, 2 Η), 7.24 (dd, 1 Η), 6.93 - 7.10 (m, 2 Η), 6.28 (dd, 1 Η), 6.09 (s, 1 Η), 5.62 (dd, 1 Η), 5.40 -5.79 (m, 1 Η), 4.24 (t, 1 Η), 4.15 - 4.21 (m, 1 Η), 4.00 (d, 1 Η), 3.92 (d, 1 Η), 3.50 - 3.69 (m, 1 Η), 2.56 - 2.71 (m, 2 Η), 2.04 - 2.25 (m, 2 Η), 1.94 - 2.04 (m, 1 Η), 1.77 - 1.87 (m> 1 Η), 1.69 - 1.77 (m, 1 Η), 1.52 - 1.66 (m, 2 II), 1.50 (s, 3 H), 1.00 (s, 3 H) LC-MS (ESI P〇S): 575.21 (MH+) ia]D23 =5 + 31.76 (c 0.25, MeOH) 表12化合物係如先前對化合物19〇所述,始於酸159及適當 烷化劑製備: [表 12] or 結構式 產率 分析 〇 rrtc, LC-MS (ESI POS): 582.25 MH+ [alo25 = + 40.00 (c 0.2, MeOH) JH NMR (300 MHz, DMSO-dfi) ppm 7.30 - 7.42 (m, 2 H), 18% 7.24 (dd,lH), 6.90-7.12 (rn, 2 H), 6.28(dd,lH), 6.00-6.15 (m, 1H), 5^6 (dd,lH), 5.40- 5.86(m,lH),4.49(m,2H), P 4.18-4.29 (m,lH),4.20(t,l H), 3.49-3.71 2.97- 3.25 (m, 2 H), 2.55-2.70(111,2 H),1.92-2.31(m,3H),1.80-1.92 (m,lH), 1.65-1.80 (m,l H), 1.51-1.65 (m, 2 H), 1.49 (s,3H),0.96(s,3H) 191 101108588 186 201247697 192 rW1 。靡T F 29% LC-MS (ESI POS): 618.16 MH+ [ot]D25 =十 46.50 (c 0.2, MeOH) 'HNMR (300 MHz, DMSO-d<i) ppm 7.30 -7.48 (ms 2 H), 7.23 (dd, 1 H),6.80-7.12(ra,2H), 6.29 (dd, 1 H), 6.08 (s, 1 H), 5.63 (dd, 1 H), 5.46 -5.77 (m, 1 H), 4.23 (t, 1 H), 4.12-4.32 (m, 1 H), 3.88 (d, 1 H), 3.81 (d, 1 H), 3.58 (q, 1 H), 2.60 -2.71 (m,2F〇, 1.93-2.30 (ra, 3 H), 1.67 - 1.89 (m, 2 H), 1.49 (s, 3 H), 1.33-1.67 (m, 2 H), 0.96 (s, 3 H) 193 HiN^ ^rcl 15% LC-MS (ESI POS): 593.3 MH+ [a]〇2S = +45.10(c 0.2, DCM) 'H NMR (300 MHz, DMSO-di) ppm 7.48 (br. s., 1 H), 7.35 (d, 2 H), 7.25 (d, 1 H), 7.02 (d, 2 H), 6.90 - 7.15 (m, 1H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.37 - 5.79 (m, 0 H), 5.58 (d, 1 H), 4.03 - 4.34 (m, 2 H), 3.47 - 3.63 (m, 4 H), 2.63 (d, 3 H), 2.22 (d, 1 H), 2.05-2.16 (m, 1 H), 1.94 (d, 1H), 1.64-1.84 (m, 1 H), 1.49 (s, 3 H), 1.31-1.64 (ra,2H), 0.96 (s,3H) 187 101108588 201247697 194 28% LC-MS (ESI POS): 574.2 MH+ [α]〇25 = + 56.7 (c 0.5, MeOH) lH NMR (300 MHz, DMSO-de) ppm 7.30 -7.44 (m, 2 H), 7.24 (dd, 1 H), 6.93 - 7.07 (m, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.58 (dd, 1 H), 5.40 -5.75 (m, 1 H), 4.21 (t, 1 H), 4.11 -4.27 (m,l H), 3.60-3.71 (m, 2 H), 3.50-3.62 (m, 1 H), 3.09 (t, 1 H), 2.55 - 2.69 (m, 2 H), 2.17-2.31 (m, 1 H), 2.03-2.17 (m, 1 H), 1.92-2.03 (m, l H), 1.80-1.90 (m, 1 H), 1.67-1.81 (m,l H), 1.51 -1.65 (m, 2 H), 1.49 (s, 3 H), 0.97 (s, 3 H) 195 * 8% LC-MS (ESI POS): 622.19 MH+ [a]D2S = + 65(c0.3, MeOH) 'H NMR (300 MHz, DMSO-de) ppm 7.37 (m, 2 H), 7.24 (d, 1 H), 7.07 (m, 2 H), 6.29 (dd, 1 H), 6.09 (s, 1H), 5.59 (d,lH), 5.46 - 5.79 (ra, 1 H), 4.23 (t, 1 H), 4.02 - 4.35 (m, I H),3.61 (dq,2H), 2.55-2.72 (m, 2 H), 2.04 - 2.29 (m, 5 H), 1.67 - 2.04 (m, 5 H),1.50(s,3H),1.37-1.67 (m, 2 H), 0.97 (s, 3 H) 188 101108588 201247697 196
49% LC-MS (ESI POS): 592.19 MH+ [a]Dis = + 31.4 (c 0.21, MeOH) 'H NMR (300 MHz, DMSO-d6) ppm 7.30 - 7.45 (m, 2 H), 7.25 (dd# 1 H), 6.91 - 7.08 (m, 2 H), 6.29 (dd, 1 H), 6.08 (s, 1 H), 5.61 (dd, 1 H), 5.43 - 5.80 (m, 1 H), 4.19-4.29 (m, 1 H), 4.18 (t, 1 H), 3.87 (d, 1 H), 3.79 (d, 1 H),3.54 (q,lH),2.55-2.71 (m, 2 H), 2.22 - 2.31 (m, 1 H), 2.20 (s, 3 H), 2.02-2.16 (m, 1 H), L85-2.00 (m,2H), 1.64-1.80 (m, I H), 1.51 -1.64 (m, 2 H),1.50(s,3H),0.95(s,3H) [實施例24]
基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12--t- eg 搭烯并[2,l-a]菲-6b-羧酸曱基酯(化合物181)之製備
於氮氣環境下159 (290毫克,0.558毫莫耳)溶解於無水 DMF ’添加N-曱基味琳(73.6微升,0.669毫莫耳)及HATU (233毫克’ 0.614毫莫耳)及混合物於室溫攪拌丨小時。添加曱 醇(250微升,6.18毫莫耳)及混合物於6〇艺加熱3小時及於室 溫隔仪。又添加曱醇(400微升,9.86毫莫耳)及混合物於6〇。〇 擾拌4小時。反應混合物以水稀釋及形成之固體藉過滤回 189 101108588 201247697 收。所得固體於乙腈濕磨,然後藉製備性HPLC純化(乙腈/ 水不含TFA)獲得標題化合物(55毫克,18.5%產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.26 - 7.33 (m, 2 H), 7.26 (dd, 1 H), 6.87 - 7.04 (m, 2 H), 6.29 (dd, 1 H), 6.09 (s, 1 H), 5.52 - 5.78 (m, 1 H), 5.51 (dd, 1 H), 4.16 - 4.25 (m, 1 H), 4.12 (t, 1 H), 3.69 (t, 1 H), 3.65 (s, 3 H), 2.80 (dd, 1 H), 2.55 - 2.68 (m, 1 H), 2.18 - 2.26 (m, 1 H), 2.05 - 2.18 (m, 1 H), 1.94 - 2.05 (m, 1 H), 1.78 - 1.92 (m, l H), 1.66 - 1.79 (m, 1 H), 1.52 - 1.64 (m, 2H), 1.50 (s,3H), 0.96 (s, 3 H) LC-MS (ESI POS): 534.11 (MH+) [a]D25 = + 35 (c 0.34; MeOH) 表13列舉之化合物係如先前對化合物197所述,始於酸159 及適當親核基團,諸如醇、胺或胺鹽,或金屬硫醇酸鹽製備: [表 13] 化合物 結構式 產率 分析 ^CN C| 13% LC-MS (ESI POS): 572.28 MH+ [a]〇2S = + 7.3(c 0.3, MeOH) *H NMR (300 MHz, DMSO-d6) ppm 7.31 (d, 2 H), 7.26 198 (d, 1H), 7.00 (d, 2 H), 6.29 (dd, 1H), 6.09(s, 1H), 5.56-5.65 (m,lH), 5.45-5.80 (m, 1 H), 4.45 (d,lH), 4.28 (d,l H), 4.18-4.27 (m,lH), 4.08 (dd, 1H), 4.02 (q,lH), 3.38 (s,3H), 2.64 (dd, 2 H), 2.05-2.30 (m, 3 H), 1.62 -1.94 (m, 2H), 1.50(s,3H),1.34-1.61 (m,2H),0.99(s,3H) 190 101108588 201247697 LC-MS (ESI POS): 550.26 MH+ [a]D25 = + 66.2 (c 0.2, DCM) 1 V *H NMR (300 MHz, DMSO-de) ppm 7.29 - 7.46 (m, 2 H), 7.24 (dd, 1 H), 6.88 - 7.08 199 30% (in, 2 H), 6.28 (dd, 1 H), 6.08 (s, 1 H), 5.52 - 5.82 (m51 H), 5.50(dd, 1 H), 4.16-4.26 P (m, 1 H), 4.17 (t, 1 H), 3.52 -3.65 (m, 1 H), 2.55 - 2.67 (m, 2 H), 2.22 (s, 3 H), 1.92 -2.19 (m, 3 H), 1.81-1.91 (m, 1 H), 1.65 - 1.81 (m, 1 H), 1.51 - 1.65 (m, 2 H), 1.49 (s, 3 H), 0.95 (s, 3 ΗΊ [實施例25]
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-(2-溴-乙醯 基)-8-(4-氣-苯基)-4b,12-二默-5-經基-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫 戊搭烯并[2,l-a]菲-2-酮(化合物200)之製備 曱烷績酸181 (653毫克’ 1.067毫莫耳)溶解於乙腈(2〇毫 升)’添加溴化四丁基銨(344毫克,1.067毫莫耳)及混合物於 8〇°C加熱6小時’然後於室溫隔夜。又添加溴化四丁基銨(344 笔克’ 1.067笔莫耳)及混合物又於80 C授掉2小時。反應混 合物分溶於水及乙酸乙酯。有機層經分離,以硫酸鈉脫水及 濃縮。粗產物藉二氧化矽凝膠急速層析術純化(洗提劑 191 101108588 201247697 DCM/AcOEt 8/2至7/3)獲得標題化合物(630毫克,1.055毫莫 耳,99%產率)。 LC-MS (ESI POS): 596.0 (MH+) (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-乙醯基-8-(4-氯-苯基)-4b,12-二氟-5-羥基-4a,6a-二曱基 -43,仆,5,6,63,61),8,9,9&,10,1〇1101),11,12-十四氫-7,崎-8-吖- 戊搭烯并[2,l-a]菲-2-酮(化合物201)之製備 190 (373毫克,0.625毫莫耳)及碘化鈉(937毫克,6.25毫莫 耳)於丙酮(17毫升)之混合物於u〇°C於微波照射下加熱3小 時。又添加額外碘化鈉(468毫克,3.12毫莫耳)及混合物於微 波照射下又加熱3小時。反應混合物分溶於乙酸乙酯及飽和 硫代硫酸鈉溶液。有機層以水洗滌,以硫酸鈉脫水及濃縮。 粗產物藉一氧化>6夕凝膠急速層析術純化(洗提劑 DCM/MeOH=99/l),然後藉製備性HPLC純化(CH3CN/H20不 含TFA)獲得標題化合物(31毫克,0 060毫莫耳,產率)。 H NMR (300 MHz,DMSO-d6) ppm 7.29 · 7.43 (m, 2 Η),7·27 (dd,1 H), 6.94 - 7.08 (m, 2 H), 6.29 (dd, 1 H), 6.09 (s, 1 H), 5.52 - 5.75 (m, l H), 5.51 (d, 1 H), 4.16 - 4.30 (m, 1 H), 4.09 (t, i H), 3.51 - 3.64 (m, 1 H), 2.62 -2.70 (m, 1 H), 2.61 (dd, 2 H), 2.20 (s, 3 H), 2.04 - 2.19 (m, 2 H), 1.82 (d, 1 H), 1.59 - 1.74 (ra, 1 H),1.51 - 1.59 (m, 2 H),1.50 (s,3 h), 0.89 (s, 3 H) LC-MS (ESI POS): 518.2 (MH+) [a】D25 = + 65.2 (0.072, CHC13) [實施例26] 101108588 192 201247697
(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基 ,2,4\41),5,6,6&,8,9,9&,10,1〇3,101),11,12-十四氫-7-4-8-。丫_戊 搭烯并[2,l-a]菲-6b·羧酸1,1-二甲基-炔丙-2-基酯(化合物2〇2) 之製備 於159 (450毫克,〇_865毫莫耳)、碳酸鉋(282毫克,0.865 毫莫耳)’碘化銅(I) (16.48毫克’ 0.087毫莫耳)及碘化鉀(230 毫克’ 1.385毫莫耳)於無水DMF (4毫升)之混合物内添加3-氣-3-曱基丁-1-炔(178毫克,1.731毫莫耳)及反應混合物於室 溫攪拌隔夜。加入乙酸乙酯及所形成之固體經過濾出;加水 及有機相以鹽水洗滌,以硫酸鈉脫水及濃縮。粗產物藉二氧 化矽凝膠急速層析術純化(洗提劑:DCM/MeOH,98/2)及於 蒸發去除溶劑後,所得固體以乙醚濕磨,過濾及於減壓下乾 燥獲得標題化合物(200毫克,0.341毫莫耳,39.4%產率)。 'H NMR (300 MHz, DMSO-d6) ppm 7.22 - 7.35 (m, 2 Η), 7.25 (dd, 1 Η), 6.75 - 7.07 (m, 2 Η), 6.28 (dd, 1 Η), 6.09 (s, 1 Η), 5.53 - 5.7S (m, 1 Η), 5.51 (ds 1 Η), 4.19 (d, 1 Η), 4.07 (t, 1 Η), 3.55 - 3.80 (m, 1 Η), 3.50 (s, 1 Η), 2.83 (dd, 1 Η), 2.54 - 2.61 (m, 1 Η), 2.19 - 2.33 (m, 1 Η), 1.82 - 2.18 (m, 3 Η), 1.67 - 1.82 (m, 1 Η), 1.63 (s, 3 Η), 1.58 (s, 3 Η), 1.55 (m, 2 Η), 1.51 (s, 3 Η), 1.03 (s, 3 Η) LC-MS (ESI POS): 586.15 (MH+) [a]D25 = + 40.6 (c 0.2, DCM) 193 101108588 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4还,41),5,6,6&,8,9,93,10,1〇1101),11,12-十四氫-7-。号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸1,1-二甲基-烯丙基酯(化合物203) 之製備 202 (150毫克,0.256毫莫耳)、喹啉(9.1〇微升,0.077毫莫 耳)及5% Pd/BaS04 (15毫克)之混合物於15 pSi氫化5小時。過 濾去除催化劑及溶劑經蒸發^殘餘物藉二氧化矽凝膠急速層 析術純化(洗㈣:DCM/MeOH,98/2),然後藉製備性HpLC 純化(CACN/^O不含TFA),獲得標題化合物(37毫克,〇 毫莫耳’ 25%產率)。 【H NMR (300 MHz, DMSO-d6) ppm 7.27 - 7 32 ,U、- τ,、, .以(m> 2 H),7.25 fdH 1 Η), 6.89 - 7.01 (m, 2 Η), 6.28 (dd, 1 Η), 6.09 (s, I Η), 5.99 (dd 1 Η) 5-77 (m, 1 Η), 5.48 (dd, 1 Η), 5.20 (dd, 1 Η), 5.04 (dd, 1 Η), 4.12-4 2^ ^ _ Η), 4.05 (t> 1 Η), 3.62 (Id, 1 Η), 2.82 (dd, 1 Η), 2.55 - 2.69 (m, ϊ ' 2-26 (m, 1 Η), 2.04 - 2.18 (m, 1 Η), 1.84 - 2.04 (m, 2 Η) l 63 1 80 ' 2 ^ " 1.51 - 1.61 (m, 2 Η), 1.51 (s, 3 Η), 1.48 (s, 3 Η), 1.46 (s,3 Η), Κ〇1 LC-MS (ESI POS): 588.23 (ΜΗ+) ’ [α]〇25 = + 48.4 (c 0.2, DCM) 說明:
*NMR s =單峰 d=雙峰 101108588 194 201247697 t=三峰 q=四峰 dd=雙峰之雙峰 m=多峰 br=寬 ESI-POS=電喷灑正游離 LC-MS =液相層析術-質譜術 [本發明化合物之藥理活性] 活體内研究 [實施例27] 脂多醣(LPS)-誘發肺臟嗜中性血球增多 本發明所述化合物之作用強度及作用持續時間係遵照Am. J. Respir. Crit· Care Med. Vol 162. ppl455-1461,2000所述方 法經些微修改評估於活體内之急性肺發炎模型。 於史伯格拉利(Sprague-Dawley)雄大氣(200克)進行測試0 氣管内滴注脂多醣(LPS)結果導致於BALF中嗜中性血球 濃度有統计上有意義的增南’此乃急性進行性肺發炎之標 記。 用於產生75%抑制之糖皮質激素劑量(ED75劑量)評估測 試’化合物(0.01-1微莫耳/千克體重)於脂多醣刺激前}小時 呈懸浮液(〇.2%Tween 80於NaCl 0.9°/〇)經氣管内投予。 晝出試驗化合物對脂多醣誘生肺臟嗜中性血球增多的抑 101108588 195 201247697 制效果之劑量-反應曲線,取糖皮質激素之ED5〇劑量作為本 生物檢定分析之強度測量值。若干本發明之代表性化合物之 ED50劑量值為0.05至0.16微莫耳/千克體重。 於第二系列實驗中,針對作用持續時間之評估,於脂多醣 刺激前24小時以ED75劑量呈懸浮液經氣管内投予化合物。 最令人關注的化合物於脂多刺激前24小時投予具有活性 (抑制百分比高於50°/〇)。 試管内研究 [實施例28] 糖皮質激素受體(GR)轉位檢定分析方案 本發明化合物之GR核轉位定量測量係依據ASSAY Drug Devel.Technol·,4(3),263-272, 2006,透過新穎的以細胞為基 礎之GR轉位檢定分析於DiscoveRx (美國加州弗利蒙特 (Fremont))開發的酶片段補償(Enzyme Fragment Complementation (EFC))格式進行。 於糠皮質激素不存在下,糖皮質激素受體(GR)係駐在於細 胞溶質錯合多種蛋白質包括熱休克蛋白。 當糖皮質激素擴散通過細胞膜進入胞漿且結合至糖皮質 激素受體(GR)時,導致熱休克蛋白釋放及轉位入細胞核,於 細胞核調節基因轉錄。
DiscoveRx檢定分析使用b-半乳糖苷酶(b-gal)之EFC作為 於經過基因改造的CHO-K1生物感測器細胞内的GR-轉位指 101108588 196 201247697 標。如透過使用專有的序列加成及修改集合之設計,b-gal 之酶接受體(EA)片段駐在於細胞核。b-gal之小胜肽酶給予 體(ED)片段直接融合至GR之C-端,且於無受體傳訊之情況 下定位在胞漿。當結合至GR配體時,錯合物轉位至細胞核, 於細胞核内藉補償恢復酶活性及檢測b-gal活性。 穩定表現b-gal之NLS-酶受體片段(EA)之b-gal及GR-酶給 予體(ED)片段之CHO-K1細胞係於含5°/。二氧化碳及95%空 氣之潮濕環境下於37°C維持於F12培養基(Invitrogen,美國 加州卡思貝德(Carlsbad))。培養基含有10% FBS,2 mM L-麩胺,50單位/毫升青黴素(penicillin),50微克/毫升鏈黴素 (streptomycin) ’ 及250微克/毫升吸濕黴素(hygromycin)及500 微克/毫升 G418 (Invitrogen)。 GR-轉位係使用含有細胞膜渗透劑及beta-gal酶基質之 PathHunter檢測套件組(DiscoveRx (美國加州弗利蒙特))測 量。全部化合物皆使用ΙίΓ11至ΙΟ·6 Μ範圍之不同濃度篩檢。 檢定分析係於48孔進行(105細胞/孔)。使用經過删減之化合 物培養係於37°C進行二小時。藉添加DiscoveRx供應的套件 組之檢測緩衝液及於室溫培養1小時進行檢測。使用 CENTRO LB 960微平板讀取器(Berthold Technologies)檢測 亮度。 使用Prism-3.0版Graphpad軟體公司(美國加州聖地牙哥) 進行ED50之統計分析及測定。 101108588 197 201247697 以GR轉位檢定分析之若干本發明代表性化合物顯示具有 0.35 nM至 10 nM之EC50。 [實施例29] LPS誘導於RAW 264.7巨噬細胞之氧化氮製造之抑制作用 以巨噬細胞鼠細胞系RAW 264.7為基礎的試管内模型用 於測試本發明之糖皮質激素之抗發炎效果。 於發炎過程中,藉氧化氮合成酶之可誘導同基因型(iNOS) 產生大量氧化氮(NO)。細菌脂多聽(LPS)常用於實驗設計中 來刺激巨噬細胞的發炎反應。 細胞生長於不含酚紅之培養基(R Ρ ΜI補充熱鈍化10 %胎牛 血清,2 mM麩胺,100單位/毫升青黴素及〇.1毫克/毫升鏈黴 素)。經由細胞與LPS培養24小時至100奈克/毫升範圍之終濃 度而提引出細胞刺激作用。於LPS暴露前15分鐘藉添加此種 化合物於DMSO載媒劑(0.1%終濃度)至最終期望濃度進行 使用本發明化合物處理。至於氧化氮製造的指數,係於經過 調理之介質内藉使用Griess比色反應(J. Neuroimmunol.,150, 29-36, 2004)測量亞硝酸鹽濃度。 IC50之統計分析及測定係使用prism_3.〇版Graphpad軟體 公司(美國加州聖地牙哥)進行。於若干代表性本發明化合物 測試之IC50值為〇.〇6 nM至5.3 nM。 101108588 198
Claims (1)
- 201247697 七、申請專利範圍: 1.一種通式(I)化合物,RMCHWHH,其中山,各自獨立地為 或2 ; z為單鍵或係選自於、-〇-及-〇c(n> ; R3係選自於由下列所組成之組群: Η、齒原子、CN、0H、c_2、(Ci_C6)炫基、忙 稀基、(cvqm烧基、⑹心)炔基、及(C〆6)烧基續隨^ 及(crc6)烷基曱醯基; ) 备 及 NR4R5 ’其中心及心係獨立地選自於由 (CrC6)烷氧基所組成之組群; 土 / (c3-c8)環燒基、(CVC8)雜環絲、芳基及雜芳基 自係選擇性地經以—或多個岭子或側氧基或CN基取代; 及 R2係選自於由下列所組成之組群: 線性或分支(CrC8)炫基、(CVC6)烧氧基、((VC6)鹵烧 基’選擇性地經以-或多個CN基或鹵原子取代; 101108588 199 201247697 •(CH2)mR6 ’其中&6係選自於由下列所組成之組群: (c3-c8)環烧基、(crc8)雜環烧基、芳基、(Ci_c6)芳基烧基、 方基氧基、芳基硫基、及雜絲,其各自係選擇性地經以選 自於由下列所組成之組群中之一或多個取代基取代:侧氧 基、OH、自原子、CN、NH2、CONH2、N〇2、NHC(0)H、 線性或分支(crC6)烷基、線性或分支(CrC6)鹵烷基、線性 或分支(CrC6)烷氧基、線性或分支(c i _c6)鹵烷氧基、(c! _c6) 經基烧氧基、(crc6) i烷氧基、(crc6)烷氧基曱醯基、(crc6) 院基綾基、(CrC6)烷基磺醯基及(Cl_c6)烷基磺烷基、(crc6) 烧*氧基磺醜基、(crc6)ii烷基磺醯氧基、胺基磺醯基、(c3-c8) 環院基、(C3_C6)雜環烷基及雜芳基,其中m為0或1至3之整 數,及 X及Y獨立地為Η或鹵原子,及 其醫燊上可接受之鹽, 但限制條件為當Rl為_CH2〇H基及R2為(crc6)烷基或 (CrC8)環烷基時,X及γ為氟原子; 或其醫藥上可接受之鹽。 2.如申請專利範圍第1項之化合物,其中,立體異構源碳 之立體化學係如通式(Γ)描繪 101108588 200 201247697 Ri3.如申請專利範圍第1或2項之化合物,其中,x及γ為氟 原子。 4·如申請專利範圍第1或2項之化合物,其係屬通式(IF)化 合物,其中, R^-(CH2)n-Z-(CH2)n,-R3,其中 η為 1及η,為 0 ; Ζ為單鍵; 為氟原子; R2係選自於由下列所組成之組群: 或77支(Ci-Cs)烧基、(c^-C6)燒氧基、(C^-C^)自烧基, 選擇性地㉞乡個CN基取代; -(CH2)mR6,其中心係選自於由下列所組成之組群:(q-q) 環2、(CVC8)雜魏基、芳基、芳基氧基、芳基硫基、及 雜方土,其各自係選擇性地經以選自於由下列所組成之組群 101108588 201 201247697 中之一或多個取代基取代.側氧基、〇H、鹵原子、cn、NH2、 N〇2、線性或分支(CrQ)烷基、(crc6)烷氧基、芳基、(crC6) 羥基烷氧基、(CrC6)ii烷氧基、直鏈或分支(Ci_C6)烷氧基 曱醯基、(crc:6)烷基羧基、芳硫基、及(CrC6)烷基磺烷基, 其中m為〇或1至3之整數; 但限制條件為R2非為4-氣-苄基; 及其醫藥上可接受之鹽。 5.如申睛專利範圍第1或2項之化合物,其係屬通式(出)化 合物,Ri^-(CH2)n-Z-(CH2)n.-R3,; Z為-S-; R3為氟原子; R2係選自於由下列所組成之組群: 線性或分支(CrC8)縣、(CrC6齡基、(Μ)祕基, 選擇性地經以-或多個⑶基麵原子取代; •(CH2)mR6,其中R顧自於由下列所組成之崎:⑸ 環烧基、㈣)雜賴基、芳基、芳基氧基、芳基硫基、及 101108588 202 201247697 雜芳基’其各自係選擇性地經以選自於由下列所組成之組群 中之一或多個取代基取代:侧氧基、〇H、鹵原子、CN、Nh2、 N〇2、線性或分支(crC6)烷基、線性或分支(Cl_C6)鹵烷基、 線性或分支(crC6)烷氧基、芳基、(Cl_c6)羥基烷氧基、(Ci_C6) 鹵烷氧基、(CrC6)烷氧基曱醯基、(Crc6)烷基羧基、芳硫 基、及(CVC6)烧基磺烷基,其中@為〇或1至3之整數; 但限制條件為&既非為4_氣-苄基也非為丙基_笨; 及其醫藥上可接受之鹽。 6·如申請專利範圍第阳項之化合物,其係屬通式(im)化 合物,其中, R1 為-(CH2)n-Z-(CH2)n,_R3 ’ 其中,為 1 ; Z為單鍵; R3 為-OH ; R2係選自於由下列所組成之組群: 線性或分支(Crc8)烷基; _(CH2)mR6 ’其tR6係選自於由(c”c8)環烧基所組成之組 群’其中m為0或1至3之整數,及 101108588 203 201247697 其醫藥上可接受之鹽β 7.如申請專利範圍第1或2項之化合物,其係屬通式(IN)化 合物,其中, Ri 為-(CH2)n-Z-(CH2)n,-R3,其中 η為0及η’為 1 ; Ζ為單鍵; R3 為-ΟΗ ; R2為-(CH2)mR6,其中R6為芳基其係選擇性地經以選自於 由下列所組成之組群中之一或多個取代基取代:齒原子、 CN、CONH2、NHC(0)H、線性或分支(CrC6)烷基、(CrC6) 烷基磺醯基、線性或分支(CrC6)鹵烷基、線性或分支(CrC6) 鹵烷氧基、(CrC6)烷氧基曱醯基、(CrC6)烷氧基磺醢基、 (CrC6)函烷基磺醯氧基、(c3_c8)環烷基、(c3-c6)雜環烷基、 胺基磺醯基、及雜芳基,及m為0,及 其醫藥上可接受之鹽。 8.如申請專利範圍第1或2項之化合物,其係為: (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:f*-丁基)-4b,12-^一氣-5-經基-6b-(2 -經基-乙酿基)-4a,6a-二曱基 101108S88 204 201247697 -4汪,41?,5,6,6&,61),8,9,93,10,1(^,101),11,12-十四氫-7-。号,8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,l〇bS,12S)-4b,12-二 氟 -8-(4-氟苄基)-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4汪,41?,5,6,6&,613,8,9,9110,1〇3,101),11,12-十四氫-7-»号-8_吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆尺,58,6&8,6乜11,9&8,10&8,1(^3,123)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-噻吩-2-基甲基 -4&,41),5,6,68,613,8,9,9&,10,1(^,101),11,12-十四氫-7-«号-8_吖-戊搭烯并[2,l-a]菲-2-酮; (4&3,仆尺,58,6&8,65尺,9&8,1〇38,1(^8,123)-413,12-二氟-8-呋 喃-2-基曱基-5-經基-6b-(2-經基-乙醯基)-4a,6a-二曱基 -4狂,413,5,6,6161),8,9,9&,10,10\1013,11,12-十四氫-7-«号,8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4汪,仆,5,6,6161?,8,9,9&,10,1(^,1013,11,12-十四氫-7,崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; 3-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-2-侧氧基 -2,4\41),5,6,6&,613,9,93,10,1〇11013,11,12-十四氫-7,崎-8-吖-戊搭烯并[2,l_a]菲_8_基曱基]-苯曱酸曱基酯; 101108588 205 201247697 (438,仆尺,58,^8,66艮9&8,1〇38,1(^8,128)-8-環己基曱基 -4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a_二曱基 -4&,41?,5,6,6&,613,8,9,9&,10,1〇11015,11,12-十四氫-7-»号-8_吖-戊搭烯并P,l-a]菲-2-酮; (4&8,仆尺,58,638,6611,9&8,1(^8,1(^^,128)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(4-曱基硫烷基-苄 基)-4&,41),5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8_((R,S)-第二-丁基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4&,41),5,6,6&,61),8,9,9&,10,1〇3,101),11,12-十四氫-7-崎-8-吖· 戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,58,6&8,6511,9&8,1(^8,1(^^,128)-8-環戊基曱基 -4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4&,41),5,6,6&,613,8,9,9&,10,1(^,101),11,12-十四氩-7-哼-8-吖-戊搭烯并|;2,l-a]菲-2-酮; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_4b,12-二氟 -5-羥基-6b-(2-羥基·乙醯基)-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,6&,61),9,9110,10&,1013,11,12-十四氫-7-4-8-吖-戊搭烯并[2,l-a]菲-8-基曱基]-苯曱酸第三-丁酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苄 基)-4b,12-二說-5·經基-6b-(2-經基-乙酿基)-4a,6a-二曱基 101108588 206 201247697 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4汪8,仆11,58,6&8,6511,938,10&8,1(^8,128)-413,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(1-丙基-丁 基)-4&,41),5,6,63,61),8,9,9&,10,10&,101),11,12-十四氫-7“等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,58,6&8,6511,9&8,1(^8,1(^8,128)-8-(4-第三-丁基-苄基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4汪,41),5,6,6161),8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8,吖-戊搭烯并[2,1-a]菲-2-酮; (4&8,仆11,58,6&8,6511,9&8,1(^8,1(^8,128)-413,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8·(4-丙基-苄 基)-4&,413,5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7-'»等-8, 吖-戊搭烯并[2,l-a]菲-2-酮; (4&3,仆尺,53,6&8,6匕11,9&8,10&8,1(^3,128)-8-環己基-41),12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4&,41),5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7-»等-8,吖-戊搭烯并[2,l-a]菲-2-酮; (4&5,仆11,58,6&8,6511,9&3,1(^8,1(^8,125)-41),12-二氟-5-羥 基-6b-(2-羥基-乙酼基)-4a,6a-二曱基-8·(3-甲基-丁 基)-43,413,5,6,6&,61),8,9,9&,10,10&,1013,11,12-十四氫-7-〇号-8-吖-戊搭烯并[2,l-a]菲-2-酮; 101108588 207 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_4b,12-:‘-5j^ 基-6b-(2-經基-乙酿基)-4a,6a-二甲基-8-(5-曱基硫烧基塞吩 -2-基曱基)-4&,仆,5,6,6\615,8,9,9&,10,10&,101),11,12-十四氫 _7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-曱 基-丙基)-4b,12-二氟(-5-經基-6b-((S)-2 -經基-乙酿基)-4a,6a-二曱基-48,41),5,6,6161),8,9,9&,10,1〇3,101),11,12-十四氫-7-崎 -8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-丁氧基-苄 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 •4&,41?,5,6,63,615,8,9,9&,10,10\1013,11,12-十四氫-7-哼-8-吖-戍搭稀弁[2,1-a]菲-2-1同; (438,仆11,53,6&3,6511,938,10&8,1(^8,128)-8-(2-環己基-乙 基)_4b,12-二敗-5-經基-6b-(2-經基-乙酿基)-4a,6a·二曱基 -4&,41?,5,6,6&,613,8,9,93,10,10&,1013,11,12,十四氫-7-吟-8-吖-戍搭稀并[2,1-a]菲-2-嗣; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基 -6b-((S)-2-羥基-乙醯基)-4a,6a-二曱基-8-(1 -曱基-1H-。引哚 -3-基曱基)-4&,41),5,6,6&,61),8,9,9110,1(^,1015,11,12-十四氫 7-噚-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&3,仆11,53,633,补11,9&8,1(^3,1(^8,128)-8-二環[2.2.1]庚 -2-基-4b,12-二氟-5-羥基-6b_(2-羥基-乙醯基)-4a,6a-二曱基 101108588 208 201247697 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-噚-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-6b-(2-經基-乙醢基)-4a,6a-二曱基-8-(3-0比咬-3-基-丙 基)-4&,仆,5,6,6&,613,8,9,9&,10,1(^,101),11,12-十四氫-7_咩-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4&8,仆11,58,6&8,6511,9&8,1(^3,1(^8,123)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a_二甲基-8·(3,3,3-三氟-丙 基)-43,仆,5,6,6&,613,8,9,9&,10,1〇3,101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,牝11,53,6&8,6511,9&8,10&8,1(^8,128)-41),12-二氟-5-羥 基-6b-(2 -經基-乙酿基)-8-(2 -°米吐-1 -基-乙基)_4a,6a- —曱基 -43,41),5,6,6&,61),8,9,9\10,1〇1101),11,12-十四氫_7-»等,8-吖-戊搭烯并[2,l-a]菲·2-酮; (4aS,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b-(R)-氟-12-氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-喹啉-5-基甲基 -4丑,41),5,6,6161?,8,9,93,10,1〇1101),11,12-十四氫-7-4-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,牝11,58,638,6511,9&8,1〇38,1(^8,128)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-噻唑-2-基曱基 -4\41),5,6,6\61?,8,9,9&,10,10&,101),11,12-十四氫-7-"等-8-吖-戊搭烯并[2,l-a]菲-2-酮; 101108S88 209 201247697 曱烷磺酸2-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苄基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4\41),5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7-»号-8-吖-戊 搭烯并[2,l-a]菲-6b·基]-2-側氧基-乙基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b·乙醯基-8-(4-氣·苄基)-4b,12-二氟-5-羥基-4a,6a-二甲基 -4&,41),5,6,61613,8,9,9&,10,10&,101),11,12-十四氫-7-«等_8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苄 基)-4b,12-二氟-5-羥基-4a,6a-二甲基_2_侧氧基 -2,4&,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-»等-8_吖-戊 搭烯并[2,l_a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_8-(3,3-:f*-丁基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氣基 -2,4\41?,5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7-«»等-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-氟-苄基)-5·羥基-4a,6a-二甲基-2-侧氧基 -2,43,41),5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4牡3,仆尺,53,638,6511,9&8,10&8,1(^8,123)-41},12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-噻吩-2-基甲基 101108588 210 201247697 -2,4\41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7_呤-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4&8,仆尺,53,638,6611,938,1(^8,1(^8,123)-41),12-二氟-8-呋 喃-2-基甲基-5-經基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,618,9,9&,10,10\101),11,12-十四氫-7-4-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4&3,仆11,58,6&8,6匕11,9&8,10&8,1(^3,128)-415,12-二氟-5-羥 基-4a,6a-二曱基-8-(5-曱基-β塞吩-2-基甲基)-2·側氧基 -2,4\413,5,6,63,8,9,9&,10,1〇3,1013,11,12-十四氩-7-崎-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:a-5-· 基-8-(4-曱氧基-节基)-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,618,9,9屯10,10&,101},11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二甲基-8-(3-曱基-丁基)-2-側氧基 -2,4\413,5,6,63,8,9,9&,10,10\101?,11,12_十四氫-7-»号-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4&8,朴11,58,6&8,汕11,9&8,1(^8,1(^8,128)-8-環戊基曱基 -4b,12-二氣-5-輕基-4a,6a-二甲基-2-側氧基 -2,4&,41),5,6,63,8,9,9110,10\101?,11,12-十四氫-7_4-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; 101108588 211 201247697 (4&8,仆尺,58,6&3,6匕11,9&8,1(^8,1(^8,123)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-(4-丙基-苄 基)-2,4\41),5,6,618,9,9&,10,1(^,1013,11,12_十四氫-7-»号-8-吖 -戊搭稀并[2,l-a]菲-6b-叛酸; (4&3,仆11,58,6&8,6511,9&8,10&8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二曱基-8-(3-甲基-苄基)-2-側氧基 -2,4\41),5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫-7-»等-8-吖-戊 搭稀并[2,1-a]菲-6b-叛酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(5-氣噻吩-2-基曱基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,48,413,5,6,618,9,9&,10,10\1013,11,12-十四氫-7-«»等-8_吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4&3,仆11,53,633,6511,9&8,1(^8,1(^3,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-8-(4_甲基-苄基)-2-側氧基 -2,4屯41),5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7-4-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4汪8,牝11,58,633,6611,9&8,1〇38,1(^3,123)-8-(4-第三-丁基-苄基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,48,41),5,6,63,8,9,93,10,10&,101),11,12_十四氫,7-°号-8-〇丫-戊 搭烯并[2,l-a]菲-6b-羧酸; (4汪8,仆11,58,6&3,6511,9&3,10&8,1(^3,128)-413,12-二氟-5_羥 基-4a,6a-二曱基-2-側氧基-8-(2-苯基硫烷基-乙 101108588 212 201247697 基)-2,4&,413,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-崎-8-吖 -戊搭烯并[2,1-a]菲-6b-羧酸; (4&8,仆尺,58,6&8,6611,9&3,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基·8-(1-丙基-丁 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+ralL-7-#-8-4 -戊搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二曱基-2·側氧基-8-(2-苯氧基-乙 基)-2,4&,扑,5,6,63,8,9,9&,1051(^,1013,11,12-十四氫-7-。号-8-吖 -戊搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(5-氯-呋喃-2-基曱基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,仆,5,6,如,8,9,9&,10,1(^,101),11,12-十四氫-7-碍-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4&8,仆尺,53,如8,6511,9&8,1(^8,1(^8,128)-8-環己基-41),12-二氟> -5-經基-4a,6a-二曱基-2-侧氧基 -2,4\41),5,6,63,8,9,9&,10,1(^,1013,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2_ 乙基丁 基)-4b,12-二乳-5·經基-4a,6a-二曱基-2-侧氧基 -2,4&,413,5,6,63,8,9,9&,10,1(^,1015,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; 101108588 213 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-丁氧 基-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41?,5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4- 丁氧基-苄 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,仆,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-"等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4汪8,仆尺,58,635,6匕11,9&8,10&8,1(^3,123)-413,12-二氟-5-羥 基-4a,6a-二甲基-8-(5-曱基-呋喃-2-基曱基)-2-側氧基 -2,4\41),5,6,63,8,9,9&,10,1〇1101),11,12-十四氫-7-碍-8-吖_戊 搭烯并[2,l-a]菲-6b-羧酸; (4&3,仆尺,53,6&3,6匕11,9&8,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-8-(5-曱基硫烷基-噻吩-2-基甲基)-2-侧氧基 -2,4&,仆,5,6,63,8,9,9&,10,1〇3,1013,11,12-十四氫-7,》等-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(l-乙基-2-曱 基-丙基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 _2,4&,扑,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7“等-8-吖-戊 搭稀并[2,l-a]菲-6b-敌酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5-· 基-4a,6a-二曱基-2-側氧基-8-(3,3,3-三氟-丙 10110858S 214 201247697 基)-2,4巳,413,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-'1号-8-吖 -戊搭烯并[2,l-a]菲-6b-羧酸; (4压8,仆11,58,6&3,6611,9&8,10&8,1(^3,128)_8-環丙基曱基 -4b,12-二氟-5-經基-4a,6a-二曱基-2-侧氧基 -2,4&,仆,5,6,6&,8,9,9&,10,10\101),11,12-十四氫-7-«号-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4&8,仆11,58,6&8,6511,9&8510&8,1(^3,128)-8-(2-環己基-乙 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41},5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-4-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4&8,仆尺,58,6&8,6511,9&8,1(^8,1(^3,128)_8-二環[2.2.1]庚 -2-基-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 _2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-4-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4&8,仆尺,58,6&8,6011,9&8,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-8-(1-曱基-1H-吲哚-3-基曱基)·2-側氧基 -2,4汪,413,5,6,6&,8,9,9&,10,10屯1013,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4汪8,仆11,53,6&8,6511,9&851(^8,1(^8,123)-8-(4-氯-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基_2_側氧基 -2,4&,41),5,6,6&,8,9,9&,10,10\1013,11,12-十四氫-7^等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-(2-側氧基-[1,3]二崎嗦-4-基) 101108588 215 201247697 酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苄 基)-4b,12-二敦-5-經基-4a,6a-二曱基-2-側氧基 -2,43,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-4,8-吖-戊 搭烯并[2,14]菲_61)-羧酸曱氧基-曱基-醯胺; (4&3,仆11,53,如8,6511,9&3,1(^8,1(^3,123)_41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基_8- β塞吩-2-基甲基 -2,4&,41?,5,6,6&,8,9,93,10,1〇3,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -8-(4-氟·苄基)-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\413,5,6,6日,8,9,9&,10,1〇11013,11,12-十四氫-7-»号-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -8-(4-氟-¥基)-5-羥基-4a,6a-二甲基-2-側氧基 _2,4&,41?,5,6,6&,8,9,9压,10,1(^,101),11,12-十四氫_7-»等,8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氰基曱基酯; (4珏5,仆尺,58,^8,6匕11,9&8,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-噻吩-2-基曱基 -2,4&,41),5,6,63,8,9,9&,10,1〇3,101),11,12-十四氫,7-»号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氰基曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-8-呋 101108588 216 201247697 喃-2-基曱基-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41?,5,6,68,8,9,9&,10,10\1013,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S·氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -8-(4-氟-苄基)-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,6&,8,9,9已,10,1(^,101),11,12-十四氫-7^等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5-· 基-4a,6a-二曱基-2-側氧基-8-噻吩-2-基曱基 -2,4\413,5,6,6&,8,9,9&,10,1〇3,101?,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:f*-丁基)-4b,12_二氣-5-經基-4a,6a-二甲基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,1-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆11,58,6&8,6511,9&8,10&8,1(^3,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-侧氧基-8-(5·甲基-噻吩-2-基曱 基)-2,4&,41),5,6,6&,8,9,9&,10,103,101),11,12-十四氫,7-'^-8,吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4江8,仆11,58,6&8,66尺,9&8,1(^3,1(^3,128)-41),12-二氟-5-羥 基-8-(4-曱氧基-苄基)-4a,6a-二甲基-2-側氧基 -2,4&,413,5,6,618,9,9&,10,1(^,101),11,12-十四氫_7-4-8-吖-戍 101108588 217 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:a-5j^ 基-4a,6a-二曱基-8-(3-曱基-丁基)-2-側氧基 -2,4&,41),5,6,6&,8,9,93,10,10&,101),11,12-十四氫-7-«号-8-吖-戊 搭烤并[2,l-a]菲-6b-硫代叛酸S-敗曱基S旨, (4&8,扑11,58,^5,65尺,9&8,1(^8,1(^8,128)-8-環戊基曱基 -4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基 -2,4&,41>,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-哼-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S·氟曱基酯; (4&3,仆11,58,688,6511,9&8,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(4-丙基-节 基)-2,4日,41),5,6,6&,8,9,9&,10,1〇3,101),11,12-十四氫-7-«号-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12_ 二氟-5-羥基 -4a,6a-二曱基-8-(3-曱基-节基)-2·側氧基 -2,43,41),5,6,63,8,9,9&,10,103,101),11,12-十四氫-7-«等-8-〇丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-((S)-氟曱基)g旨; (4日8,仆11,58,6&8,65尺,9&8,10&8,1058,128)-41),12-二氟-5-經 基-4a,6a-二甲基-2-側氧基-8-(5-氣-β塞吩-2-基-曱 基)-2,4\41),5,6,6&,8,9,9&,10,1〇8,101),11,12-十四氫-7-崎-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 101108588 218 201247697 基-4a,6a-二曱基-8-(4-曱基-苄基)-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+ralL-7-4,8dY-A 搭烯并[2,l-a]菲-6b-硫代羧酸S·氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-丁基-节基)-4b,12-二氣-5-經基-4a,6a-—曱基-2-側氧基 -2,4&,413,5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_4b,12-二氟-5-羥 基-4a,6a-二曱基-2-侧氧基-8-(2-苯基硫烷基-乙 基)_2,4&,41),5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-噚-8-吖 -戊搭烯并[2,l_a]菲-6b-硫代羧酸S-氟甲基酯; (4&8,仆11,58,6&3,6511,933,10&8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-(1-丙基-丁 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-哼-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4&8,仆11,58,6&3,6511,938,1〇38,1(^8,123)-41),12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(2-苯氧基-乙 基)-2,4\41),5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7,》号-8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4&8,仆11,58,6&8,6511,933,1(^8,1053,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-(5-氯-n夫喃-2-基-曱 基),2,4\41),5,6,618,9,9&,10,1〇11013,11,12-十四氫-7-。等-8-吖 101108588 219 201247697 •戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8*^&*-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,43,41),5,6,6&,8,9,93,10,10&,101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二敦-5-經基-4a,6a-二曱基-2-侧氧基 -2,43,41),5,6,6&,8,9,93,10,1〇1101),11,12-十四氫,7-«等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-第三-丁氧 基_ >基)_4b,12-二氣-5-經基-4a,6a-二曱基-2-侧氧基 -2,4\413,5,6,6已,8,9,93,10,10&,1015,11,12-十四氫-7-«号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4&8,仆11,53,6&8,6511,9&8,10&8,1(^8,128)-8-(4_丁氧基-苄 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,43,41),5,6,618,9,93,10,10\101),11,12-十四氫-7-今-8-吖_戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆11,58,638,6511,938,1(^8,1(^8,128)-41),12-二氟-5-羥 基-4a,6a-.一曱基-8-(5-甲基-咬°南-2-基曱基)-2-側氧基 -2,4\413,5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-»号-8_吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 101108588 220 201247697 基-4a,6a-二甲基-2-侧氧基-(5-曱基硫烧基-β塞吩-2-基曱 基)-2,4&,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-哼-8-吖 -戊搭稀并[2,1-a]菲-6b-硫代叛酸S-氟曱基醋; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8-((S)-l-乙基-2-曱 基-丙基)_4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,415,5,6,6&,8,9,9&,10,1(^,1015,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆11,58,6&3,6611,9&8,1(^8,1(^8,128)-413,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(3,3,3-三氣-丙 基)-2,4汪,41?,5,6,6汪,8,9,9&,10,1〇3,101),11,12-十四氫-7-"等_8-吖 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4汪3,仆11,53,6&8,邰11,9&8,10&8,1058,123)-8-環丙基甲基 -4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,93,10,10&,101),11,12-十四氫-7-«号_8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4珏8,仆11,58,6&8,邰艮9&8,1(^3,1(^8,128)-8-(2-環己基-乙 基)·41),12·二乱-5-經基-4a,6a-二甲基-2-側氧基 -2,4\413,5,6,63,8,9,9&,10,10&,101),11,12-十四氫-7-哼-8-吖-戊 搭烯并[2,1-a]菲-6b-硫代羧酸S-氟曱基酯; (4日8,仆11,53,6&8,6511,9&8,1(^8,1(^8,125)-8-二環[2.2.1]庚 -2-基-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,如,8,9,9&,10,1〇1101),11,12-十四氫-7-»等-8-吖-戊 101108588 221 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥基 -4a,6a-一曱基-8-((S)-l-曱基-1Η-π引**朵-3-基-曱基)-2•側氧基 -2,4迎,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-'1等-8-'3丫-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4&8,仆11,58,6&3,6611,9&8,1(^3,1(^3,123)-41),12-二氟-61)· (2_氣-乙酿基)-5-經基-4a,6a-二曱基-8-(4-曱基-节 基)-4已,41),5,6,6&,613,8,9,9&,10,10&,101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-6b-(2_氣-乙酿基)-5-經基-4a,6a-二曱基-8-σ塞吩-2-基曱基 -4&,41),5,6,63,61),8,9,9&,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-6b-(2-氟-乙醯基)-8-(4-氟-苄基)-5-羥基-4a,6a-二曱基 -4&,41),5,6,6&,613,8,9,9&,10,1(^,101),11,12-十四氫-7“号-8-吖-戍搭稀并[2,1-a]菲-2-酉同; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -6b-(2-氣-乙酿基)-8-0夫喃-2-基曱基-5-經基-4a,6a-二曱基 -4已,41),5,6,6\61),8,9,93,10,10&,1013,11,12-十四氫-7-"号-8-吖-戍搭稀弁[2,l-a]菲-2-嗣; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 101108588 222 201247697 -6b-(2-氟-乙醯基)-5-羥基-8-(4-曱氧基-苄基)-4a,6a-二曱基 -4&,41>,5,6,6&,61),8,9,9&,10,10&,1015,11,12-十四氫-7-〇等-8-口丫-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,55,6&3,6111,9&8,10&3,10匕8,128)-8-環戊基曱基 -4b,12-二氣-6b-(2-氟j -乙酿基)-5-經基-4a,6a-二甲基 -4&,41),5,6,6&,61),8,9,9&,10,10&,101),11,12-十四氫-7-°号-8-口丫-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:f*-丁基)-4b,12-二氟-6b-(2-氟-乙醯基)_5_羥基-4a,6a-二曱基 -4&,41),5,6,6&,613,8,9,9&,10,10&,101),11,12-十四氫-7-崎-8-吖-戊搭烯并P,1-a]菲-2-酮; (4牡8,仆11,53,6&8,6匕11,9&3,1(^3,1053,128)-8-(5-氯-噻吩-2-基甲基)-4b,12-二氟-6b-(2-氟-乙醯基)-5-羥基-4a,6a-二曱基 -4壮,41),5,6,63,613,8,9,93,10,10\101),11,12-十四氫-7-崎-8-吖· 戍搭稀弁[2,l-a]菲-2-嗣, (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-5-· 基-6b-(2-經基-乙酿基)-8-[4-(2-經基-乙氧基)·节基]-4a,6a-二 曱基-4\41),5,6,6\61),8,9,9\10,103,101),11,12-十四氫-7-嘮-8-°丫-戍搭婦弁[2,l-a]菲-2-酿1, (4狂8,仆11,53,638,6511,9&8,1(^8,1(^3,128)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-"等,8-吖- 101108588 223 201247697 戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基_6b-(2-羥基-乙醯基)-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12·十四氫-7_ 崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,朴11,58,6&3,6511,9&3,1(^3,1(^8,128)-413,12-二氟-5-羥 基-6b-(2-羥基·乙醯基)_4a,6a-二甲基-8-對-曱苯基 -43,41?,5,6,6&,613,8,9,9&,10,10&,1013,11,12-十四氫^7-呤-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,53,638,补11,9&8,1(^3,1058,128)-413,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-喹啉-6-基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-n 等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a_二甲基-8-吡啶-3-基 •4&,41),5,6,63,615,8,9,93,10,1〇1101),11,12-十四氫-7-°号-8-吖-戊搭稀并[2,l-a]菲-2-嗣, (4&8,仆11,58,6&8,6511,938,1〇38,1053,128)-413,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-間·曱苯基 -4&,413,5,6,63,61),8,9,93,10,10&,101),11,12-十四氫-7-“等-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4&8,仆11,58,6511,9&8,1(^8,1058,128)-41),12-二氟,8-(4-氟- 101108588 224 201247697 苯基)-5-經基-6b-((S)_2-經基-乙酿基)-4a,6a-二曱基 -43,41^,5,6,63,61),8,9,9&,10,1(^,1013,11,12-十四氫-7-«号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣-苯 基)-4b,12-二氣-5-經基-6b-(2-輕基-乙酿基)-4a,6a-二曱基 -4&,41),5,6,63,613,8,9,9&,10,10&,101),11,12-十四氫-7-«号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-5-· 基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-(4-三氣曱基-苯 基)-4&,41?,5,6,6&,613,8,9,9&,10,1(^,1013,11,12_十四氫-7-,-8-吖-戊搭烯并[2,1-a]菲-2-酮; (433,仆11,58,6511,933,1(^3,1(^^,128)-41),12-二氟-8-(3-氟-本基經基-6b-((S)-2-經基·乙酿基)-4a,6a-二曱基 -48,41),5,6,63,613,8,9,9&,10,1〇3,101),11,12-十四氫,7-«号-8_吖-戊搭稀并[2,l-a]菲-2-嗣, (4牡3,仆11,53,638,6511,9&8,1〇38,1058,123)-413,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-鄰-曱笨基 -4已,41),5,6,6161),8,9,93,10,1(^,1013,11,12-十四氫-7-»号-8-吖· 戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6bR,9aS,10aS,10bS,12S)-8_(4-氣-3-甲基-苯 基)-4b, 12·二亂-5-經基-6b-((S)-2-經基-乙酿基)-4a,6a-二曱 基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-«号-8-吖 101108588 225 201247697 -戊搭烯并[2,l-a]$M-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-3-三氟 甲基·苯基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二 甲基-4&,仆,5,6,以,61),8,9,93,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,4-二氣-苯 基)-4b,12-二敦-5-經基-6b-(2-經基-乙醯基)-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7“等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,牝11,58,如8,6511,988,1(^8,1(^8,128)-8-(4-溴-苯基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-«»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS)-4b-氟-5-羥基 •6b-(2-羥基-乙醯基)-4a,6a-二甲基-2·側氧基 -2,43,41?,5,6,6&,61),9,9110,10\101?,11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯曱腈; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基-乙酿基)-4a,6a-二甲基-2-側氧基 -2,4\413,5,6,6&,613,9,9&,10,1(^,101?,11,12-十四氫,7-4-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯曱醯胺; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5-· 101108588 226 201247697 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(4-三氟曱氧基-笨 基)-4阻,41?,5,6,6&,61),8,9,9&,10,10&,101),11,12-十四氫-7-崎-8- 吖·戊搭烯并[2,l-a]菲-2-酮; 曱烷磺酸4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氣5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基·2-側氧基 •2,4\413,5,6,6&,61),9,9&,10,1(^,101),11,12-十四氫-7-哼-8-吖-戊搭烯并[2,l-a]菲-8_基]-苯基酯; (4&8,仆尺,58,以8,6匕艮9巳831(^8,1%8,128)-8-(4-環己基-苯 基)-4b,12 -二氣-5 -經基-6b_(2 -經基-乙酿基)-4a,6a-二曱基 -4已,41),5,6,6&,61),8,9,9&,10,10\101),11,12_十四氫-7-»号-8-吖· 戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,58,6&8,6511,9&8,10&8,1(^8,128)-41?,12-二氟-5-羥 基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-(4-嗔吩-2-基本 基)-4\41>,5,6,如,61),8,9,9110,10&,101),11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基-乙酿基)-4a,6a-二甲基-2-侧氧基 -2,4&,41),5,6,6161?,9,9&,10,1〇1101),11,12-十四氫-7-«等-8-吖-戊搭烯并[2,l_a]菲各基]-苯曱酸曱基酯; (433,仆11,58,6&8,6511,9&8,10&8,1(^8,128)_413,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-8-(4-曱烷磺醯基-苯基)-4a,6a-二曱 基-4&,41),5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7-口号-8-吖 101108588 227 201247697 -戊搭稀并[2, l-a]菲-2-嗣; 3- [(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-2·側氧基 2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,ll,12-十四氫吖· 戊搭烯并[2,l-a]菲-8-基]苯曱腈; 4- [(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,ll,12-十四氫-7-»等-8-吖-戊搭稀并[2,l-a]菲-8-基]-苯續酿胺; (4&8,仆11,58,633,6511,9&3,10&8,1058,128)-8-(4-環丙基-苯 基)-4b,12-二敗-5 -經基-6b-(2 -經基-乙酿基)-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-f5-T*-苯基)-4b,12-二氣-5 -經基-6b-(2-經基-乙酿基)-4a,6a·二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫,7-«»号 _8·0丫-戊搭烯并[2,l-a]菲-2-酮; N-{4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氣-5 -經基-6b-(2·經基-乙酿基)-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,6&,61),9,9&,10,10\1013,11,12-十四氫-7-«»号-8-吖-戊搭烯并[2,l-a]菲-8-基]-苯基}-曱醯胺; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-5-· 101108588 228 201247697 基-6b-(2-羥基-乙醯基)-4a,6a-二甲基-8-(3-三氟曱基-苯 基)-4&,41?,5,6,6&,61),8,9,9&,10,10&,101?,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&5,仆11,53,6&8,6匕11,9&8,1〇38,1(^8,128)-仆,12-二氟-5_羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(3-三氟曱氧基-苯 基)-4\41),5,6,6&,61),8,9,9110,1(^,101),11,12-十四氫-7-»等-8_ 吖-戊搭烯并P,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-溴-苯 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 •4&,41?,5,6,63,61),8,9,9110,1(^,101},11,12-十四氫-7-吟-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-苯并噻唑-6· 基-4b,12-.一氣-5-經基-6b-(2-經基-乙酿基)-4a,6a-二曱基 -4牡,413,5,6,如,613,8,9,9\10,10\101?,11,12-十四氳-7-»号-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4&8,仆尺,58,6&8,6匕11,9&8,1(^8,1(^8,123)-物,12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-8-(4-羥基-苯基三氟曱烷磺酸 根)-4a,6a-二曱基-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12- + 四氫-7-哼-8-吖戊搭烯并[2,l-a]菲-2-酮; (4&8,仆尺,58,6&8,6匕11,93891(^8,1(^8,128)-8-(3-環丙基-笨 基)-4b,12-二氟-5-羥基-6b-(2-羥基·乙醯基)-4a,6a-二曱基 -4\41),5,6,6161),8,9,9&,10,1〇11013,11,12-十四氫-7-»号-8-吖- 101108588 229 201247697 戊搭烯并P,l-a]菲-2-酮; (438,仆尺,58,6&8,6匕11,9&8,1(^8,1(^3,128)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-(4-哌啶-4-基曱基-苯 基)-4&,41),5,6,6&,61),8,9,9&,10,10&,101),11,12-十四氫-7“等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-5-g 基 -4a,6a- 二甲基 -2- 侧氧基 -8- 苯基 -2,4&,41),5,6,618,9,93,10,1〇110|3,11,12-十四氳-7-«等-8-吖-戊 搭稀并[2,1-a]菲-6b-叛酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基 •2,4&,41),5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基 -2,4\41),5,6,6汪,8,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖-戊 搭稀并[2,1-a]菲-6b-叛酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-5-g 基-4a,6a-二曱基-2-侧氧基-8-間-曱苯基 -2,4\413,5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫-7-"等-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 101108588 230 201247697 基-4a,6a-二曱基-2-側氧基-8-鄰·曱苯基 -2,4&,413,5,6,63,8,9,9&,10,10&,101),11,12-十四氫-7-«号,8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-對-曱苯基 -2,4&,仆,5,6,6巳,8,9,9&,10,10&,101),11,12-十四氫-7-«号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS510aS,10bS,12S)-8-(3-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41^,5,6,6&,8,9,93,10,10&,101),11,12-十四氫-7_«号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -8-(4-鼠-苯基)-5-經基-4a,6a-二曱基-2-側氧基 -2,4&,仆,5,6,618,9,9&,10,1(^,1013,11,12-十四氫-7-吟-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS510aS,10bS,12S)-4b,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8- 0比。定-3-基 -2,4&,仆,5,6,6&,8,9,9&,10,10这,101),11,12_十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS510aS,10bS,12S)-4b,12-二 氟 -8-(3-說-苯基)-5-經基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 101108588 231 201247697 搭稀并[2, l-a]菲-6b-叛酸; (4&8,仆11,58,633,6511,933,10&8,1058,123)-413,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(4-三氣曱基-苯 基)-2,4&,41),5,6,6&,8,9,93,10,1(^,101),11,12-十四氮-7-崎-8_吖 -戊搭烯并[2,l-a]菲-6b-羧酸; (4&8,仆尺,58,6&8,处11,938,10&5,1(^8,128)-41),12-二氟-5-羥 基 -4a,6a- 二甲基 -2- 側氧基 -8- 苯基 -2,4\415,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-»号,8-吖-戊 搭烯并[2,l-a]菲-6b_硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\仆,5,6,6&,8,9,9\10,10&,101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5’S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12_ 二氟-5·羥 基-4a,6a-二曱基-2-側氧基-8-間-曱本基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-»号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S·氟甲基酯; (4&8,仆11,58,6&3,6611,9&8,10&8,1(^5,128)-41),12-二氟-5-羥 基-4a,6a-二甲基-2-側氧基-8-鄰-曱本基 -2,4&,仆,5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-碍-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&3,仆11,58,如3,6511,9&8,1(^8,1(^3,128)-41),12-二氟-5-羥 101108588 232 201247697 基-4a,6a-二曱基-2·側氧基-8-對-曱苯基 -2,4&,41),5,6,6&,8,9,9&,10,1〇3,101),11,12-十四氫-7-哼-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,618,9,9&,10,10&,1013,11,12-十四氫-7-«等-8-吖_戊 搭稀弁[2,1-a]菲-6b-硫代叛酸S-氣曱基醋; (4&5,仆尺,58,6611,9&8,1(^8,1(^3,128)-413,12-二氟-8-(4-氟-苯基)_5_羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,618,9,9&,10,1〇11013,11,12-十四氫-7-«等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-((S)-氟甲基)酯; (4&8,仆11,58,6&3,65义,9&8,1〇38,1(^3,128)-413,12-二氟-5-羥 基·43,63··二曱基-2-侧氧基-8- 0比0定-3-基 -2,4&,41?,5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫_7-#-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4&8,仆尺,58,6511,9&8,10&8,1(^8,128)-41),12-二氟_8-(3-氟-苯基)-5-羥基-4a,6a-二甲基-2-側氧基 -2,4&,41),5,6,618,9,98,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-((S)-氟曱基)酯; (4阻3,仆11,58,633,66尺,9&8,10&8,1(^8,123)-41?,12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-(4-三氟曱基-苯 基)-2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+ralL-7_4-8-V 101108588 233 201247697 -戊搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二 氟 -6b-(2-氟-乙醯基)-5-羥基-4a,6a-二曱基-8-苯基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-«等-8-吖-戊搭稀弁[2,1-a]菲-2-明, (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12- 一氣-6b-(2-氣-乙酿基)-5-經基-4a,6a-二曱基 -4&,41),5,6,6&,613,8,9,9110,10&,101),11,12-十四氫-7-«号-8-吖-戊搭烯并[2,1-a]菲-2-酮; 曱烷磺酸2_[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 _2,4&,41),5,6,6&,8,9,9&,10,10&,101),11,12,十四氫-7-»等-8-吖-戊 搭烯并[2,1 -a]菲-6b-基]-2-侧氧基-乙基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-(2-氯-乙醯 基)-8-(4-氯-苯基)-4b,12-二氟-5-羥基-4a,6a-二曱基 ,4\415,5,6,6&,61),8,9,9&,10,10&,1013,11,12-十四氫-7-'^-8-吖-戊搭烯并[2,l-a]菲-2-酮; (438,牝尺,58,6&8,66艮9&8,1(^8,1(^8,128)-8-(4-氣-苯基)-4b,12-二氟-5-羥基-4a,6a-二曱基-6b-(2-曱基硫烷基-乙酿 基)-43,41),5,6,6&,61),8,9,93,10,1〇11013,11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&3,牝11,58,6&8,6511,9&8,1(^8,1(^8,123)-8-(4-氣-苯基)- 101108588 234 201247697 4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氯曱基硫酯; (4&3,朴11,53,如8,6511,9&8,10&8,1(^8,128)-8-(4-氯-苯基)-4b,12-二氣-5-經基-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,63,8,9,9&,10,1(^,101),11,12-十四氫-7-»等-8,吖-戊 搭烯并[2,l-a]菲-6b-羧酸環丙基曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-經基-4a,6a-二曱基-2-側氧基 •2,4&,41),5,6,6&,8,9,98,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氰基曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,43,413,5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-°号-8-°丫-戊 搭烯并[2,l-a]菲-6b-羧酸胺基曱醯基曱基酯; (4aS,4bR,5S,6aS,6bR,9aS510aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5·羥基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-4-8-吖戊 搭烯并[2,l-a]菲-6b-羧酸2,2,2-三氟-乙基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-侧氧基 -2,4&,413,5,6,6&,8,9,93,10,1(^,101),11,12-十四氫-7*-号-8-。丫-戊 101108588 235 201247697 搭烯并[2,l-a]菲-6b-羧酸2-氟-乙基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12- 一敦-5-經基-4a,6a-二甲基-2-側氧基 2,4日,41),5,6,6&,8,9,9已,10,1(^,101),11,12-十四氫-7-今-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氰基曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基 -2,43,41),5,6,63,8,9,93,10,1〇3,101),11,12-十四氫-7-»号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-(2-氟-乙基)醋; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,43,413,5,6,63,8,9,93,10,1〇1101),11,12-十四氫-7-<^-8-吖-戊 搭烯并[2,1 -a]菲-6b-硫代羧酸S-(2,2,2-三氟-乙基)醋; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b, 12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b, 5,6,6a, 8,9,9a,10,10a, 10b, 11,12-十四氩-7-4-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-胺基曱醯基曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二乳-5-經基-4a,6a-二甲基-2-側氧基 •2,4\413,5,6,63,8,9,93,10,103,101),11,12_十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-丙-2-炔基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 101108588 236 201247697 基)-4b,12-二敗-5-沒基-4a,6a-二曱基-2·側氣基 -2,4\415,5,6,6&,8,9,9&,10,10&,1015,11,12-十四氫-7-"号-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-環丁基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-崎-8-吖-戊 搭稀并[2,1 -a]菲-6b-硫代竣酸S-(2-側氧基-丙基)酉旨; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,93,10,1〇1101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a·二曱基-2_側氧基 -2,4&,41?,5,6,6&,8,9,9&,10,10&,1013,11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氰基曱基-甲基-醯胺; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4\413,5,6,6&,8,9,9&,10,1〇1101),11,12-十四氫-7,崎-8_吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-乙醯基-8-(4-氣-苯基)-4b,12-二氟-5-羥基-4a,6a-二甲基 -4&,41),5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7“号-8-吖- 101108588 237 201247697 戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苯 基)-4b,12-二氟-5-羥基-4a,6a-二甲基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-n等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸1,1-二曱基-丙-2-炔基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苯 基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基 -2,4&,415,5,6,6&,8,9,9&,10,1(^,1013,11,12-十四氫-7-"号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸1,1-二曱基-烯丙基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:f*-丁基)-4b,12-二氟-5-羥基_6b-(2-羥基-乙醯基)-4a,6a-二甲基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»等-8-吖-戊搭烯并[2,1-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-氟-苄基)-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4&,41),5,6,63,61),8,9,9110,103,101),11,12-十四氫-7-"等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&3,牝11,58,638,6611,938,10&3,1(^3,128)_41),12-二氟-5-羥 基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-嗟吩-2-基曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (438,仆艮58,6&8,6511,9&8,1(^8,1058,123)-413,12-二氟-8-呋 101108588 238 201247697 喃-2-基曱基-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7-°等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(2-乙基-丁 基)-4b,12-二氣-5-經基-6b-(2_經基·乙酿基)-4a,6a- —曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7_0 等-8-吖-戊搭烯并[2,l-a]菲-2-酮; 3-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基-乙醯基)-4a,6a-二曱基-2-侧氧基 -2,4a,4b,5,6,6a,6b,9,9a,10,10a,10b,l 1,12-十四氫-7-»号-8_ 吖-戊搭烯并[2,l-a]菲-8-基曱基]-苯曱酸曱基酯; (4日8,仆11,58,638,6匕11,938,1(^8,1(^8,128)-8-環己基曱基 •4b,12-二鼠-5-輕基-6b-(2-經基-乙酿基)-4a,6a- —曱基 -4&,41),5,6,6&,61),8,9,9&,10,10&,1013,11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,53,683,6511,9&8,1(^8,1(^^,123)-41),12-二氟-5-羥 基-6b-(2-經基-乙酿基)-4a,6a-二曱基-8-(4-曱基硫烧基-卞 基)-4\41?,5,6,6&,61),8,9,9110,1(^,101?,11,12-十四氫-7-嘮-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-((R,S)-第二-丁基)-4b,12 -二氣-5-經基-6b-(2 -經基-乙酿基)-4a,6a·二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,l 1,12-十四氫-7·» 等-8-吖- 101108588 239 201247697 戊搭烯并[2,1-a]菲-2-酮; (433,仆尺,58,638,6511,9&8,1(^3,1(^8,128)冬環戊基曱基 -4b,12-二 I -5-經基-6b-(2-經基-乙醢基)-4a,6a-二曱基 -4\413,5,6,6\61),8,9,9110,1〇1101),11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; 4-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -5-經基-6b-(2-經基·乙酿基)-4a,6a-二曱基-2-側氧基 -2,4&,413,5,6,6&,613,9,9&,10,103,101),11,12-十四氫-7,《号-8-吖-戊搭烯并[2,l-a]菲-8-基曱基]-苯曱酸第三-丁基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苄 基)-4b,12-二氟l -5_經基-6b-(2-經基-乙酿基)-4a,6a-二曱基 -43,41),5,6,63,61),8,9,9&,10,1(^,101),11,12-十四氫-7-4-8-吖-戊搭烯并[2,l-a]菲-2·酮; 曱烷磺酸2-[(4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-側氧基 -2,4&,41),5,6,618,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖-戊 搭烯并P,1 -a]菲-6b-基]-2-側氧基-乙基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-6b-乙醯基-8·(4-氣-苄基)-4b,12-二氟-5-羥基-4a,6a-二曱基 -4\41),5,6,6161),8,9,9&,10,1(^,1013,11,12-十四氫-7-»等-8-吖-戊搭烯并I;2,l-a]菲-2-酮; (4&8,仆11,58,6&8,6511,9&8,1〇33,1058,123)-8-(4-氯-苄基)- 101108588 240 201247697 4b, 12-二氟-5-經基-4a,6a-二曱基-2-側氧基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+E9lL-7-a|-8-4j 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:fS-丁基)-4b,12-二氟-5-羥基-4a,6a-二曱基-2-侧氧基 -2,4&,41>,5,6,6&,8,9,9&,10,1〇3,101),11,12-十四氫-7-°等冬口丫-戊 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -8-(4-氣-节基)-5_經基-4a,6a-—曱基-2-側氧基 -2,4&,41),5,6,6&,8,9,93,10,10&,1015,11,12-十四氫-7“号-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4&8,牝11,58,6&8,6511,9&8,1(^8,1058,128)-41),12-二氟-5-羥 基-4a,6a-二曱基-2-側氧基-8-噻吩-2-基甲基 -2,4\41),5,6,63,8,9,9&,10,1(^,101),11,12-十四氫-7-〇号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸; (4汪8,仆11,53,6&8,65尺,9&3,1(^8,1(^3,128)-41),12-二氟-8-呋 喃-2-基曱基-5-經基-4a,6a-二曱基-2-側氧基 -2,4\413,5,6,6&,8,9,9&,10,10屯101),11,12-十四氫-7-。等-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氯-苄 基)-4b,12-二氟-5·羥基-4a,6a_二甲基-2-側氧基 -2,43,41),5,6,6&,8,9,9&,10,10&,101),11,12-十四氫-7-哼-8-吖-戊 101108588 241 201247697 搭烯并[2,l-a]菲-6b-硫代羧酸S-(2-側氧基-[1,3]二哼嗦-4-基) 酯; (4&8,扑尺,58,6&3,6611,933,1(^8,1(^8,128)-8-(4-氣-苄基)-4b, 12- 一氣-5-經基·4&,6&-二曱基_2_側氧基 _2,4\41),5,6,618,9,9&,10,1〇1101),11,12-十四氫-7-崎-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸曱氧基-曱基-醯胺; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:l-5-· 基_4a,6a-二曱基-2-側氧基-8-嗟吩-2-基甲基 -2,4\41),5,6,618,9,9&,10,10屯101),11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氟曱基酯; (4&8,仆11,53,6&8,6511,9&8,10&3,1(^8,128)-413,12-二氟-8-(4-氟-苄基)-5-羥基-4a,6a-二甲基-2-側氧基 -2,4\41?,5,6,618,9,9&,10,1〇11013,11,12-十四氫-7-«»等-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_4b,12-二氟 -8-(4-氟-苄基)_5_羥基-4a,6a-二曱基-2-側氧基 -2,4\41),5,6,63,8,9,9&,10,10\1013,11,12-十四氫-7^号-8-吖-戊 搭烯并[2,l-a]菲-6b-羧酸氰基甲基酯; (4巳3,仆11,53,633,6511,9&8,1(^8,1(^5,128)-41),12-二氟-5-羥 基_4a,6a-二曱基-2-側氧基-8- °塞吩-2-基曱基 -2,4a,4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-+ra&-7-»f-8-々4 搭烯并[2,l-a]菲-6b-羧酸氰基曱基酯; 101108588 242 201247697 (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:‘-8·^ °南-2-基曱基-5-經基-4a,6a-二曱基-2-側氧基 -2,4a, 4b,5,6,6a,8,9,9a,10,10a,10b,ll,12-十四氫-7-4-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)_4b,12-二氟 -8-(4-氟-节基)-5-經基-4a,6a-二曱基-2-側氧基 -2,43,413,5,6,6&,8,9,93,10,10\1013,11,12-十四氫-7,崎-8-吖-戊 搭烯并[2,1-a]菲_6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12·二氟-5-羥 基-4a,6a-二曱基-2·側氧基-8-噻吩-2-基曱基 -2,4&,41),5,6,6&,8,9,9&,10,10&,1015,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:f*-丁基)-4b,12-二敗-5-經基-4a,6a-二曱基-2-側氧基 _2,4\41),5,6,6&,8,9,9&,10,1〇3,1013,11,12-十四氫-7-»等-8-吖-戊 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟曱基酯; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-二氟 -6b-(2-氟-乙醯基)-5-羥基-4a,6a-二曱基-8-(4-曱基-苄 基)-4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫7-哼-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,朴11,58,如8,6611,9&8,10&3,1(^3,128)-413,12-二氟-61> (2-氟-乙醯基)-5-羥基-4a,6a-二曱基-8-噻吩-2-基曱基 101108588 243 201247697 _4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-崎-8-吖-戊搭烯并P,l-a]菲-2-酮; (435,仆11,58,6&3,6511,938,1〇38,1(^8,128)-41),12-二氟-61)-(2-氟-乙醯基)-8-(4-氟-苄基)-5-羥基-4a,6a-二甲基 -4&,413,5,6,6161),8,9,93,10,10\1013,11,12-十四氫-7-»号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&3,仆11,58,688,65艮9&8,1(^8,1(^5,128)-41),12-二氟-61> (2-氟-乙醯基)-8-呋喃-2·基曱基-5-羥基-4a,6a-二甲基 -4&,41),5,6,6\61),8,9,93,10,1(^,101),11,12-十四氫-7-崎-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆11,53,6&8,6511,933,1〇38,1(^8,128)-413,12-二氟-61)-(2-氟-乙醢基)-5-羥基-8-(4-甲氧基-苄基)-4a,6a-二甲基 -4&,415,5,6,6日,61?,8,9,93,10,103,101),11,12-十四氫-7-»号-8-吖-戊搭烯并[2,l-a]菲-2-酮; (438,牝11,58,6&8,6511,9&8,10&8,1(^8,128)-8_環戊基甲基 -4b, 12- 一 氣-6b-(2-氣-乙酿基)-5-經基-4a,6a-二甲基 -4&,41),5,6,63,613,8,9,93,10,1〇3,101),11,12-十四氫-7-崎,8-吖-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(3,3-:f*-丁基)-4b,12-二氟-6b-(2-氟-乙醯基)-5-羥基-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12_ 十四氫-7-» 等_8_吖-戊搭烯并[2,l-a]菲-2·酮; 101108588 244 201247697 (4&8,朴尺,58,638,65艮9&8,10&8,1(^3,128)-8_(5-氣-噻吩-2-基曱基)-4b,12-二氟-6b-(2-氟-乙醯基)-5-羥基-4a,6a-二曱基 -4a,4b,5,6,6a,6b,8,9,9a,10,10a,10b,ll,12-十四氫-7-»等-8-吖-^ 戊搭烯并P,l-a]菲-2-酮; ,, (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12_:l-5々^ 基-6b-(2-經基-乙酸基)-8-[4-(2-經基-乙氧基)-午基]-4a,6a-二 曱基-4\41),5,6,6161),8,9,9&,10,1〇1101),11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,扑11,58,6&8,65艮9&8,1(^3,1(^8,128)-41),12-二氟-5-羥 基-6b-(2-羥基-乙醯基)-4a,6a-二曱基-8-苯基 -4牡,413,5,6,6&,61),8,9,93,10,10&,101),11,12-十四氫-7->1等-8-〇丫-戊搭烯并[2,l-a]菲-2-酮; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-8-(4-氣-笨 基)-4b,12-二氟-5-羥基-6b-(2-羥基-乙醯基)-4a,6a-二甲基 _4巳,41),5,6,6&,61),8,9,9&,10,1(^,101),11,12-十四氫-7-»等-8-吖-戊搭烯并[2,l-a]菲-2-酮; (4&8,仆尺,58,6&8,6七11,9&8,1(^8,1(^8,123)-41),12-二氟-5-羥 基 -4a,6a- 二甲基 -2- 侧氧基 -8- 苯基 " -2,4\41),5,6,6&,8,9,9&,10,10\101),11,12-十四氫-7-噚-8-吖-戊 搭烯并[2,1-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,l〇bS,12S)-8-(4-氣-笨 基)-4b,12-二氟j -5-經基-4a,6a-二曱基-2-側氧基 101108588 245 201247697 _2,4&,仆,5,6,6&,8,9,9\10,1(^,101),11,12-十四氫_7_〇号_8_〇丫戍 搭烯并[2,l-a]菲-6b-羧酸; (4aS,4bR,5S,6aS,6bR,9aS,10aS,10bS,12S)-4b,12-:HM 基-4a,6a-.一 曱基_2_側氧基苯芙 搭烯并[2,l-a]菲-6b-硫代羧酸S-氟甲基酯; 或其醫藥上可接受之鹽。 9. 一種醫藥組成物,其係包含申請專利範圍第丨至8項中任 一項定義之化合物,連同一或多個醫藥上可接受之載劑及/ 或賦形劑。 10. —種組合物,其係包含申請專利範圍第1至8項中任一 項定義之化合物,與一或多個選自於下列類別之活性成分: (32-促效劑、抗蕈毒鹼劑、皮質類固醇、有絲分裂原活化蛋 白質激酶(P38 MAP激酶)抑制劑、核因子κ-Β激酶亞單元 β(ΙΚΚ2)抑制劑、人類嗜中性細胞彈性蛋白酶(HNE)抑制 劑、磷酸二酯酶4(PDE4)抑制劑、白三烯調節劑、非類固醇 抗發炎劑(NSAID)、及黏液調節劑。 11. 如申請專利範圍第1或2項之化合物,其係用作為藥物。 12. 如申凊專利範圍第1或2項之化合物,其係用於預防及/ 或治療其中涉及發炎細胞之數目、活性及移動的減少之任何 疾病。 13. 如申請專利範圍第1或2項之化合物,其係用於預防及/ 101108588 246 201247697 或治療呼吸系疾病。 14. 如申請專利範圍第1或2項之化合物,其係用於預防及/ 或治療氣喘及慢性阻塞性肺病(COPD)。 15. —種裝置,其係包含申請專利範圍第9項之醫藥組成 物,該裝置可以是單劑或多劑乾粉吸入器、定量劑量吸入 器、或軟霧喷霧器。 101108588 247 201247697 四、指定代表圖: (一) 本案指定代表圖為:無 (二) 本代表圖之元件符號簡單說明: 無 五、本案若有化學式時,請揭示最能顯示發明特徵的化學式:101108588 2
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US9155747B2 (en) * | 2012-09-13 | 2015-10-13 | Chiesi Farmaceutici S.P.A. | Isoxazolidine derivatives |
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