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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250419생성일: 2026년 10월 27일

Triethylamine → [(6-Benzyloxy-1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-methyl-amino]-acetic acid

https://huagongshe.com/reaction/250419

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl N-methylaminoacetate hydrochlorideHCID 171173—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물6-Benzyloxy-1-chloro-4-hydroxy-isoquinoline-3-carboxylic acidHCID 18698135—
용매DichloromethaneHCID 6344—
용매Sodium HydroxideHCID 14798—
생성물[(6-Benzyloxy-1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-methyl-amino]-acetic acidHCID 86595476—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863292B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-d07e5e5d752c43978edda116f3d29690
출처 메모uspto-grants-2011_01