Hydrochloric Acid → 1-(cyclopropylmethyl)-2-[(5-ethoxy-2-pyridinyl)methyl]-1H-benzimidazole-5-carboxylic acid
반응식
[CH:1]1([CH2:4][N:5]2[C:9]3[CH:10]=[CH:11]C(C#N)=[CH:13][C:8]=3[N:7]=[C:6]2[CH2:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH3:25])=[CH:19][N:18]=2)[CH2:3][CH2:2]1.[CH3:26][CH2:27][OH:28].[OH-:29].[K+].Cl>O>[CH:1]1([CH2:4][N:5]2[C:9]3[CH:10]=[CH:11][C:26]([C:27]([OH:29])=[O:28])=[CH:13][C:8]=3[N:7]=[C:6]2[CH2:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH3:25])=[CH:19][N:18]=2)[CH2:3][CH2:2]1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution 1-(cyclopropylmethyl)-2-[(5-ethoxy-2-pyridinyl)methyl]-1H-benzimidazole-5-carbonitrile (400 mg, 1.203 mmol) in 1:1 EtOH:H2O (12 mL) was added KOH (269 mg, 4.81 mmol). The resulting mixture was refluxed for 36 h. The mixture was acidified with 1 N HCl to pH˜6.0. The precipitate (397 mg, 94%) was used in the subsequent step without further purification. MS (ESI) (M+H)+=352.
후처리
- temperatureThe resulting mixture was refluxed for 36 h
- customThe precipitate (397 mg, 94%) was used in the subsequent step without further purification
출처 및 근거
- ORD 기록
- ord-c9f235c845d743e785a361029dc9dee4
- 출처 데이터셋
- uspto-grants-2006_04
- 특허 번호
- US07030139B2
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