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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1762123생성일: 2026년 10월 26일

Triethylamine → 3-(3-[[[(Phenylmethoxy)-amino]-carbonyl]-amino]-4-methoxyphenyl)-1-trifluroacetyl piperidine

https://huagongshe.com/reaction/1762123

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzyloxyamine hydrochlorideHCID 102312—
반응물3-(3-Isocyanato-4-methoxyphenyl)-1-trifluoroacetyl-piperidineHCID 20042559—
용매DichloromethaneHCID 6344—
생성물3-(3-[[[(Phenylmethoxy)-amino]-carbonyl]-amino]-4-methoxyphenyl)-1-trifluroacetyl piperidineHCID 1421063985.2%

반응 단계

1.68 g of O-benzyl-hydroxylamine hydrochloride suspended in 30 ml of methylene chloride were added to 1.52 ml of triethylamine and then 3.2 g of the product of Step A in 10 ml of methylene chloride were added dropwise with stirring for 2 hours, followed by evaporating to dryness under reduced pressure. The residue was chromatographed on silica, (eluent: methylene chloride-ethyl acetate 96-4) to obtain 3.75 g of the expected product melting at 134° C. after crystallization from a 1-1 mixture of methylene chloride and isopropyl ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04831043
출처 데이터셋uspto-grants-1989_05
ORD IDord-c7470a822b464060a1bd302ab26dfcf5
출처 메모uspto-grants-1989_05