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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526323생성일: 2026년 10월 24일

Cesium carbonate → tert-butyl methyl 2-{(1S)-[3-(benzyloxy)phenyl][(tert-butoxycarbonyl)amino]methyl}propanedioate

https://huagongshe.com/ko/reaction/526323

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl methyl malonateHCID 2733872—
반응물1-[3,5-Bis(trifluoromethyl)phenyl]-3-[(1R,2R)-(-)-2-(dimethylamino)cyclohexyl]thiourea(R,R-TUC)HCID 11486766—
반응물HCID 71268083HCID 71268083—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl methyl 2-{(1S)-[3-(benzyloxy)phenyl][(tert-butoxycarbonyl)amino]methyl}propanedioateHCID 117653877—

반응 조건

온도0 °C

반응 단계

Tert-butyl {[3-(benzyloxy)phenyl](phenylsulfonyl)methyl}carbamate (3.0 g, 5.93 mmol) was suspended in a toluene (21.6 mL) water (16 mL) mixture. At 0° C. tert-butyl methyl malonate (1.2 mL, 7.1 mmol), cesium carbonate (1.94 g, 5.9 mmol) and 1-[3,5-bis(trifluoromethy) phenyl]-3-[(1R,2R)-(−)-2-(dimethylamino)cyclohexyl]thiourea (246 mg, 0.59 mmol) was added and the mixture was stirred for 72 hours at 0° C. After storage at −20° C. for 72 hours the mixture was diluted with water and ethyl acetate, after filtration the phases were separated and the aqueous phase extracted with ethyl acetate. The combined extracts were dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (ethyl acetate in hexane 0 to 35%) to yield 2.17 g of enantiomerically enriched tert-butyl methyl 2-{(1S)-[3-(benzyloxy)phenyl][(tert-butoxycarbonyl)amino]methyl}propanedioate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09345793B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-91abd16de4f848ec89b86b9eb7815cf1
출처 메모uspto-grants-2016_05