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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 708643생성일: 2026년 10월 25일

Dichloromethane → (S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester 7-methyl ester

https://huagongshe.com/reaction/708643

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(S)-6-amino-7-hydroxy-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl esterHCID 59337426—
반응물[4-(3,4-Dichloro-benzyloxy)-phenyl]-oxo-acetaldehydeHCID 86654900—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물(S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester 7-methyl esterHCID 6671939671.6%

반응 단계

[4-(3,4-Dichloro-benzyloxy)-phenyl]-oxo-acetaldehyde (616 mg) was dissolved in DCE (25 mL), and (S)-6-amino-7-hydroxy-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl ester (644 mg) and sodium triacetoxyborohydride (520 mg) were added. The mixture was stirred overnight at room temperature. DCM (50 mL) was added to the reaction mixture and poured into water (25 mL). The organic layer was washed with 10% Na2CO3 solution and brine, and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography (hexanes/ethyl acetate from 90:10 to 70:30) to give (S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester 7-methyl ester (855 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09175003B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-eaeb3fb18045404ca9cf38e33180b8b4
출처 메모uspto-grants-2015_11