반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[C:15]([Cl:19])=[N:14][C:13]([C:20]([OH:22])=O)=[C:12]2[OH:23])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.Cl.[CH3:56][NH:57][CH2:58][C:59]([O:61]CC)=[O:60]>ClCCl.[OH-].[Na+]>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[C:15]([Cl:19])=[N:14][C:13]([C:20]([N:57]([CH2:58][C:59]([OH:61])=[O:60])[CH3:56])=[O:22])=[C:12]2[OH:23])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
6-Benzyloxy-1-chloro-4-hydroxy-isoquinoline-3-carboxylic acid, 0.33 g, 0.5 ml of triethylamine, 0.400 g of HATU, and 0.165 g of ethyl N-methyl-amino-acetate hydrochloride were combined in 15 ml of dichloromethane and the reaction mixture was stirred at room temperature for 18 h to give, after silica gel chromatography, 0.232 g of an off-white solid, MS-(+)-ion: 429.0 amu. 0.208 g of this intermediate product were dissolved in 10 ml of methanolic NaOH (1.5 M) and the mixture was stirred at room temperature for 3 h. The solvent was removed with a rotary evaporator, the residue was dissolved in water, and the aqueous layer was extracted with 50 ml of ethyl acetate. The aqueous layer was acidified to pH=1 with aqueous HCl to give a solid precipitate. The solid was collected by suction filtration, washed with water, and dried in a vacuum oven (80° C.) to give 0.180 g of white solid: MS-(+)-ion: 401.0 amu.
후처리
- customto give
- stirringthe mixture was stirred at room temperature for 3 h
- customThe solvent was removed with a rotary evaporator
- dissolutionthe residue was dissolved in water
- extractionthe aqueous layer was extracted with 50 ml of ethyl acetate
- customto give a solid precipitate
- filtrationThe solid was collected by suction filtration
- washwashed with water
- customdried in a vacuum oven (80° C.)
출처 및 근거
- ORD 기록
- ord-d07e5e5d752c43978edda116f3d29690
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07863292B2
연결된 노트
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