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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43813생성일: 2026년 10월 23일

Methanol → HCID 86648758, 화합물

https://huagongshe.com/ko/reaction/43813

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Chloroacetyl chlorideHCID 6577—
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
반응물tert-Butyl cis(+/-)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylateHCID 86648489—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물HCID 86648758HCID 86648758—

반응 단계

Methanol (10 ml), ethyl acetate (10 ml) and a 4 N hydrochloric acid/ethyl acetate solution (30 mL) were added to tert-butyl cis(±)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylate obtained in Example (40a) (1.88 g, 5.16 mmol), and the mixture was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, azeotropically dehydrated by adding toluene, and dissolved in methylene chloride (100 ml), followed by adding diisopropylethylamine (2.1 g). Chloroacetyl chloride (640 mg, 5.68 mmol) was dissolved in methylene chloride (50 ml), and the solution was added dropwise at 0° C. Following the dropwise addition, the mixture was stirred at 0° C. to room temperature overnight. The reaction solution was washed with water and aqueous sodium bicarbonate, concentrated under reduced pressure, and then azeotropically dehydrated by adding toluene to obtain the title compound. Half of the resulting compound was used for the next reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d76ebe9249394468ad9fc23b0a184889
출처 메모uspto-grants-2013_09