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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391859생성일: 2026년 10월 24일

Formaldehyde → (S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1-methyl-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/ko/reaction/391859

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물DichloromethaneHCID 6344—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(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 66719396—
용매Dce thfHCID 21493386—
생성물(S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1-methyl-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester 7-methyl esterHCID 6671952190.8%

반응 단계

To a solution of (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 (298 mg) in THF/DCE (30 mL, 2:1) was added paraformaldehyde (90 mg, 4 eq.) and sodium triacetoxy-borohydride (208 mg) and the mixture stirred 4 hours. DCM was added to the mixture and the organic washed with 10% Na2CO3 solution and brine. The organic was dried over sodium sulfate and the solvent removed under reduced pressure to afford the crude amine. The residue was purified by flash chromatography (hexanes/ethyl acetate from 80:20 to 60:40) to provide the product (277 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383644B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-5081721ca0984d6580d6d7517f51df6e
출처 메모uspto-grants-2013_02