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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573007생성일: 2026년 10월 27일

1,1'-Carbonyldiimidazole → 1,1-Dimethylethyl N-((1S)-2-(methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl)carbamate

https://huagongshe.com/reaction/573007

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
용매DichloromethaneHCID 6344—
생성물1,1-Dimethylethyl N-((1S)-2-(methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl)carbamateHCID 11055945—

반응 단계

1000 mg (3.77 mmol) N-(tert-butoxycarbonyl)-L-phenylalanine was placed in 10 mL dichloromethane and mixed with 733 mg (4.52 mmol) 1,1′-carbonyldiimidazole. The batch was stirred for 15 min until the evolution of gas had stopped. Next the mixture was mixed with 441 mg (4.52 mmol) N,O-dimethylhydroxylamine hydrochloride and 657 μL (3.77 mmol) N,N-diisopropylethylamine and stirred for 1 hour at RT. Next the batch was diluted with dichloromethane and washed with distilled water, 0.5N hydrochloric acid and saturated sodium chloride solution in succession. The organic phase was separated and the combined aqueous phases were re-extracted with ethyl acetate. The combined organic phases were dried over magnesium sulfate and concentrated in vacuo, yielding 1090 mg (93% of the theoretical) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029406B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-3f716fca4ead4a42841abe5f54d6c286
출처 메모uspto-grants-2015_05