Hydrochloric Acid → 3-[({6-Amino-3,5-dicyano-4-[4-(2-hydroxyethoxy)phenyl]pyridin-2-yl}oxy)methyl]benzenecarboxylic acid
반응식
CC(C)([O-])C.[K+].[OH:7][CH2:8][C:9]1[CH:10]=[C:11]([C:15]([OH:17])=[O:16])[CH:12]=[CH:13][CH:14]=1.[NH2:18][C:19]1[C:24]([C:25]#[N:26])=[C:23]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[C:22]([C:33]#[N:34])=[C:21](SC2C=CC=CC=2)[N:20]=1.Cl.C[O:44][CH2:45][CH2:46][O:47]C>O>[NH2:18][C:19]1[N:20]=[C:21]([O:7][CH2:8][C:9]2[CH:10]=[C:11]([C:15]([OH:17])=[O:16])[CH:12]=[CH:13][CH:14]=2)[C:22]([C:33]#[N:34])=[C:23]([C:27]2[CH:28]=[CH:29][C:30]([O:44][CH2:45][CH2:46][OH:47])=[CH:31][CH:32]=2)[C:24]=1[C:25]#[N:26]참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 60 °C
실험 절차
4.72 g (42.06 mmol) of potassium tert-butoxide were suspended in 25 ml of 1,2-dimethoxyethane. After addition of 1.73 g (10.51 mmol) of 3-(hydroxymethyl)benzenecarboxylic acid (Example 66A) and 1.72 g (5.26 mmol) of 2-amino-4-phenyl-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile (Example 36A), the mixture was stirred at 60° C. overnight. After cooling of the reaction mixture, 50 ml of water were added. With ice-cooling, the clear solution was acidified to pH 6-7 using conc. hydrochloric acid. The solution was evaporated. Purification was by column chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 1/1, finally acetonitrile/water 10/1).
후처리
- additionwere added
- temperatureWith ice-cooling
- customThe solution was evaporated
- customPurification
출처 및 근거
- ORD 기록
- ord-46a0d27483334464b0612eabc200768e
- 출처 데이터셋
- uspto-grants-2015_11
- 특허 번호
- US09187428B2
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