JP2012530834A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2012530834A5 JP2012530834A5 JP2012516751A JP2012516751A JP2012530834A5 JP 2012530834 A5 JP2012530834 A5 JP 2012530834A5 JP 2012516751 A JP2012516751 A JP 2012516751A JP 2012516751 A JP2012516751 A JP 2012516751A JP 2012530834 A5 JP2012530834 A5 JP 2012530834A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- hydroxy
- heptan
- oxoacetamide
- 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
- 150000001875 compounds Chemical class 0.000 claims description 9
- -1 n- heptyl Chemical group 0.000 claims description 3
- CHCYTBNWFUCHQI-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-yl)-n-heptan-4-yl-2-oxoacetamide Chemical compound CCCC(CCC)NC(=O)C(=O)C1=CC=C2OCOC2=C1 CHCYTBNWFUCHQI-UHFFFAOYSA-N 0.000 claims description 2
- UEQBREKAZDBTBB-UHFFFAOYSA-N n-heptan-4-yl-2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound CCCC(CCC)NC(=O)C(O)C1=CC=C(O)C(OC)=C1 UEQBREKAZDBTBB-UHFFFAOYSA-N 0.000 claims description 2
- 239000000796 flavoring agent Substances 0.000 claims 3
- 235000019634 flavors Nutrition 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- WLYVUGJNTRTZIF-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-yl)-n-(2-hydroxyethyl)-2-oxoacetamide Chemical compound OCCNC(=O)C(=O)C1=CC=C2OCOC2=C1 WLYVUGJNTRTZIF-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- JMKCLAXRSXPCLQ-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-oxo-2-phenylacetamide Chemical compound OCCNC(=O)C(=O)C1=CC=CC=C1 JMKCLAXRSXPCLQ-UHFFFAOYSA-N 0.000 claims 1
- NMUQYBPDIJRAMA-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-oxopropanamide Chemical compound CC(=O)C(=O)NCCO NMUQYBPDIJRAMA-UHFFFAOYSA-N 0.000 claims 1
- YDRAJDHVSGXBGH-UHFFFAOYSA-N n-heptan-4-yl-2-(4-hydroxy-3-methoxyphenyl)-2-oxoacetamide Chemical compound CCCC(CCC)NC(=O)C(=O)C1=CC=C(O)C(OC)=C1 YDRAJDHVSGXBGH-UHFFFAOYSA-N 0.000 claims 1
- AFDKKRFCMOZKOV-UHFFFAOYSA-N n-heptan-4-yl-2-oxo-3-phenylpropanamide Chemical compound CCCC(CCC)NC(=O)C(=O)CC1=CC=CC=C1 AFDKKRFCMOZKOV-UHFFFAOYSA-N 0.000 claims 1
- ZKFBWVBIPJGTKT-UHFFFAOYSA-N n-heptyl-2-(4-hydroxy-3-methoxyphenyl)-2-oxoacetamide Chemical compound CCCCCCCNC(=O)C(=O)C1=CC=C(O)C(OC)=C1 ZKFBWVBIPJGTKT-UHFFFAOYSA-N 0.000 claims 1
- PGALUHMMKKOFDC-UHFFFAOYSA-N n-heptyl-2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound CCCCCCCNC(=O)C(O)C1=CC=C(O)C(OC)=C1 PGALUHMMKKOFDC-UHFFFAOYSA-N 0.000 claims 1
- HAKXLFCGLROTAP-UHFFFAOYSA-N n-heptyl-2-oxo-3-phenylpropanamide Chemical compound CCCCCCCNC(=O)C(=O)CC1=CC=CC=C1 HAKXLFCGLROTAP-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 235000008960 ketchup Nutrition 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- ZYJHZYNSHIMYJQ-UHFFFAOYSA-N ethyl 2-(1,3-benzodioxol-5-yl)-2-oxoacetate Chemical compound CCOC(=O)C(=O)C1=CC=C2OCOC2=C1 ZYJHZYNSHIMYJQ-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000227653 Lycopersicon Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- CLJMMQGDJNYDER-UHFFFAOYSA-N heptan-4-amine Chemical compound CCCC(N)CCC CLJMMQGDJNYDER-UHFFFAOYSA-N 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 235000019583 umami taste Nutrition 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0911000.8 | 2009-06-25 | ||
| GBGB0911000.8A GB0911000D0 (en) | 2009-06-25 | 2009-06-25 | Compounds |
| PCT/EP2010/059027 WO2010149754A1 (en) | 2009-06-25 | 2010-06-24 | Compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012530834A JP2012530834A (ja) | 2012-12-06 |
| JP2012530834A5 true JP2012530834A5 (enExample) | 2013-08-15 |
| JP5766187B2 JP5766187B2 (ja) | 2015-08-19 |
Family
ID=41008243
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012516751A Active JP5766187B2 (ja) | 2009-06-25 | 2010-06-24 | 化合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8816102B2 (enExample) |
| EP (1) | EP2445359B1 (enExample) |
| JP (1) | JP5766187B2 (enExample) |
| GB (1) | GB0911000D0 (enExample) |
| WO (1) | WO2010149754A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2723714T3 (pl) * | 2011-06-02 | 2018-02-28 | CHINOIN Zrt. | Nowe sposoby otrzymywania amidów prostaglandyn |
| EP2932858A1 (de) * | 2014-04-16 | 2015-10-21 | Symrise AG | Homovanillinsäure-Ester, insbesondere zum Erzielen eines Wärme- und/oder Schärfeeindrucks |
| US9957380B2 (en) * | 2015-04-17 | 2018-05-01 | Johns Manville | Formaldehyde-free smoke reduction agents for binders |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3121061B2 (ja) * | 1991-10-04 | 2000-12-25 | 塩野義製薬株式会社 | アルコキシイミノアセトアミド類製造用中間体の製造法およびそれに用いる中間体 |
| DE10030880A1 (de) * | 2000-06-23 | 2002-01-03 | Haarmann & Reimer Gmbh | 3,4-Dihydroxymandelsäurealkylamide und ihre Verwendung |
| DE10226942A1 (de) * | 2002-06-17 | 2003-12-24 | Symrise Gmbh & Co Kg | Verwendung von Mandelsäurealkylamiden als Aromastoffe |
| DE602005026654D1 (de) | 2004-04-20 | 2011-04-14 | Givaudan Nederland Services Bv | Geschmacksmodifiziermittel |
| JP4541126B2 (ja) | 2004-12-22 | 2010-09-08 | 花王株式会社 | ピルビン酸アミド類 |
| WO2007027095A1 (en) | 2005-09-02 | 2007-03-08 | Quest International Services B.V. | Improved flavour compositions |
-
2009
- 2009-06-25 GB GBGB0911000.8A patent/GB0911000D0/en not_active Ceased
-
2010
- 2010-06-24 US US13/378,257 patent/US8816102B2/en active Active
- 2010-06-24 EP EP10724880.9A patent/EP2445359B1/en active Active
- 2010-06-24 JP JP2012516751A patent/JP5766187B2/ja active Active
- 2010-06-24 WO PCT/EP2010/059027 patent/WO2010149754A1/en not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR20210127961A (ko) | 방법 및 화합물 | |
| TWI688558B (zh) | 一種亞托敏（Ａｚｏｘｙｓｔｒｏｂｉｎ）的製備方法 | |
| TWI653223B (zh) | 用於製備前列腺素醯胺之新穎方法（二） | |
| CN103582622B (zh) | 经由亚胺鎓盐制备双环化合物的方法 | |
| JP2015506343A5 (enExample) | ||
| JP2014503001A5 (enExample) | ||
| JP2017088632A (ja) | ベンズアミド化合物の合成に有用な化合物 | |
| JP2012530834A5 (enExample) | ||
| JP2005522478A (ja) | コンブレタスタチンの製造方法 | |
| CN104918912B (zh) | 2‑氨基‑4,6‑二甲氧基苯甲酰胺和其他苯甲酰胺化合物的合成方法 | |
| KR101728443B1 (ko) | 2-아미노니코틴산벤질에스테르 유도체의 제조 방법 | |
| CN106748966B (zh) | 一种雷米普利关键中间体的合成方法 | |
| JP6702623B2 (ja) | メデトミジンの合成に有用な３−アリールブタナールなどの化合物の調製方法 | |
| CN116023359B (zh) | 一种氨基噻吩类化合物的合成方法及氨基噻吩类化合物 | |
| US20100298574A1 (en) | Process For The Synthesis Of (+) And (-)-1-(3,4-Dichlorophenyl)-3-Azabicyclo[3.1.0]Hexane | |
| JP2018090551A (ja) | Ｌ−カルノシン誘導体またはその塩、及びｌ−カルノシンまたはその塩の製造方法 | |
| WO2018184196A1 (zh) | 一种制备2-芳基丙二酰胺的方法及其应用 | |
| JP2015511578A (ja) | 置換フェニルプロパノンを調製するためのプロセス | |
| CN108689874B (zh) | 一种制备2-芳基丙二酰胺的方法及其应用 | |
| JP2017502009A (ja) | シロドシン及びその中間体の製造方法 | |
| JP5818278B2 (ja) | ペレチノインの向上した合成 | |
| JP2023547270A (ja) | アルコール性水酸基供与体と活性水素供与体とを光延反応させる方法 | |
| JP2007515403A5 (enExample) | ||
| JP5507579B2 (ja) | Ｎ−［５−（３−ジメチルアミノ−アクリロイル）−２−フルオロ−フェニル］−ｎ−メチル−アセトアミドの調製方法 | |
| CN100404516C (zh) | 六氢哒嗪三羧酸酯的制备方法 |