반응식
CO[C:3]([C:5]1[N:6]=[C:7]([C:23]#[N:24])[C:8]2[C:13]([C:14]=1[OH:15])=[CH:12][CH:11]=[C:10]([O:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[CH:9]=2)=[O:4].[NH2:25][CH2:26][C:27]1([C:30]([OH:32])=[O:31])[CH2:29][CH2:28]1.C[O-].[Na+].Cl>CO.O>[C:23]([C:7]1[C:8]2[C:13](=[CH:12][CH:11]=[C:10]([O:16][C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH:9]=2)[C:14]([OH:15])=[C:5]([C:3]([NH:25][CH2:26][C:27]2([C:30]([OH:32])=[O:31])[CH2:29][CH2:28]2)=[O:4])[N:6]=1)#[N:24]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
After a mixture of 1-cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (101 mg, 0.318 mmol), 1-aminomethyl-cyclopropanecarboxylic acid (110 mg, 0.955 mmol, prepared according to literature: Ohno, Mitsuru et al Synlett 1991, 919-920), and NaOMe in MeOH (1.6 mL, 0.5 M solution) was microwaved at 120° C. for 1 h, the reaction mixture was cooled, diluted with water and acidified with 2 M HCl aqueous solution, the resulted solids were collected via filtration, water-washed and air-dried to give solids, which were further column purified to give the desired product (33 mg). LC MS ESI+: 404 (M+1)+.
후처리
- customwas microwaved at 120° C. for 1 h
- temperaturethe reaction mixture was cooled
- filtrationthe resulted solids were collected via filtration, water-
- washwashed
- customair-dried
- customto give solids, which
- custompurified
출처 및 근거
- ORD 기록
- ord-bd7f705b2cf4488db5ac93c66b5788fa
- 출처 데이터셋
- uspto-grants-2016_08
- 특허 번호
- US09409892B2
연결된 노트
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