JP2016028038A5 - - Google Patents
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- Publication number
- JP2016028038A5 JP2016028038A5 JP2015160176A JP2015160176A JP2016028038A5 JP 2016028038 A5 JP2016028038 A5 JP 2016028038A5 JP 2015160176 A JP2015160176 A JP 2015160176A JP 2015160176 A JP2015160176 A JP 2015160176A JP 2016028038 A5 JP2016028038 A5 JP 2016028038A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- methyl
- ether
- triisopropylsilyl
- triethylsilyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 benzyloxymethyl Chemical group 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 claims description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- FNIATMYXUPOJRW-UHFFFAOYSA-N cyclohexylidene Chemical group [C]1CCCCC1 FNIATMYXUPOJRW-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical compound CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- GXHMMDRXHUIUMN-UHFFFAOYSA-N methanesulfonic acid Chemical compound CS(O)(=O)=O.CS(O)(=O)=O GXHMMDRXHUIUMN-UHFFFAOYSA-N 0.000 description 1
- BSCCSDNZEIHXOK-UHFFFAOYSA-N phenyl carbamate Chemical compound NC(=O)OC1=CC=CC=C1 BSCCSDNZEIHXOK-UHFFFAOYSA-N 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09011146.9 | 2009-08-31 | ||
| EP09011146 | 2009-08-31 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012527221A Division JP5955769B2 (ja) | 2009-08-31 | 2010-08-25 | （１ｓ，４ｒ）−２−オキサ−３−アザビシクロ［２．２．１］ヘプト−５−エンの製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016028038A JP2016028038A (ja) | 2016-02-25 |
| JP2016028038A5 true JP2016028038A5 (enExample) | 2017-03-30 |
| JP6121492B2 JP6121492B2 (ja) | 2017-04-26 |
Family
ID=41172230
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012527221A Expired - Fee Related JP5955769B2 (ja) | 2009-08-31 | 2010-08-25 | （１ｓ，４ｒ）−２−オキサ−３−アザビシクロ［２．２．１］ヘプト−５−エンの製造方法 |
| JP2015160176A Active JP6121492B2 (ja) | 2009-08-31 | 2015-08-14 | （１ｓ，４ｒ）−２−オキサ−３−アザビシクロ［２．２．１］ヘプト−５−エンの製造方法 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012527221A Expired - Fee Related JP5955769B2 (ja) | 2009-08-31 | 2010-08-25 | （１ｓ，４ｒ）−２−オキサ−３−アザビシクロ［２．２．１］ヘプト−５−エンの製造方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US9102634B2 (enExample) |
| EP (1) | EP2473492B1 (enExample) |
| JP (2) | JP5955769B2 (enExample) |
| KR (2) | KR101758941B1 (enExample) |
| CN (1) | CN102482237B (enExample) |
| AU (1) | AU2010288864A1 (enExample) |
| BR (1) | BR112012004523A2 (enExample) |
| CA (1) | CA2772258C (enExample) |
| ES (1) | ES2556959T3 (enExample) |
| IL (1) | IL218322A0 (enExample) |
| IN (1) | IN2012DN01873A (enExample) |
| PL (1) | PL2473492T3 (enExample) |
| SI (1) | SI2473492T1 (enExample) |
| TW (1) | TWI518090B (enExample) |
| WO (1) | WO2011023374A1 (enExample) |
| ZA (1) | ZA201201715B (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1867239B1 (en) | 2005-03-11 | 2016-06-29 | Taiyokagaku Co., Ltd. | Thickening composition improved in viscosity manifestation |
| CN104114542B (zh) | 2011-12-23 | 2017-11-14 | 力奇制药公司 | 三唑并嘧啶化合物的合成 |
| WO2016189542A1 (en) | 2015-05-28 | 2016-12-01 | Natco Pharma Ltd | Novel process for the preparation of sapropterin dihydrochloride and its key intermediate, l-biopterin |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8729994D0 (en) * | 1987-12-23 | 1988-02-03 | Glaxo Group Ltd | Chemical compounds |
| US5576323A (en) | 1993-12-03 | 1996-11-19 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
-
2010
- 2010-08-25 CN CN201080038452.9A patent/CN102482237B/zh not_active Expired - Fee Related
- 2010-08-25 AU AU2010288864A patent/AU2010288864A1/en not_active Abandoned
- 2010-08-25 SI SI201031080T patent/SI2473492T1/sl unknown
- 2010-08-25 BR BR112012004523A patent/BR112012004523A2/pt not_active IP Right Cessation
- 2010-08-25 US US13/392,947 patent/US9102634B2/en not_active Expired - Fee Related
- 2010-08-25 PL PL10747830T patent/PL2473492T3/pl unknown
- 2010-08-25 JP JP2012527221A patent/JP5955769B2/ja not_active Expired - Fee Related
- 2010-08-25 ES ES10747830.7T patent/ES2556959T3/es active Active
- 2010-08-25 EP EP10747830.7A patent/EP2473492B1/en not_active Not-in-force
- 2010-08-25 KR KR1020127007771A patent/KR101758941B1/ko not_active Expired - Fee Related
- 2010-08-25 CA CA2772258A patent/CA2772258C/en not_active Expired - Fee Related
- 2010-08-25 IN IN1873DEN2012 patent/IN2012DN01873A/en unknown
- 2010-08-25 WO PCT/EP2010/005199 patent/WO2011023374A1/en not_active Ceased
- 2010-08-25 KR KR1020177003043A patent/KR20170015575A/ko not_active Ceased
- 2010-08-27 TW TW099128784A patent/TWI518090B/zh not_active IP Right Cessation
-
2012
- 2012-02-26 IL IL218322A patent/IL218322A0/en not_active IP Right Cessation
- 2012-03-08 ZA ZA2012/01715A patent/ZA201201715B/en unknown
-
2015
- 2015-08-14 JP JP2015160176A patent/JP6121492B2/ja active Active
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