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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393216생성일: 2026년 10월 24일

Sodium borohydride → HCID 131724622, 화합물

https://huagongshe.com/ko/reaction/393216

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물methyl (3R,4R)-1-[3-(2,3,5-trifluorophenyl)prop-2-ynyl]-4-[3-hydroxyimino-3-(6-methoxyquinolin-4-yl)propyl]piperidine-3-carboxylateHCID 136380444—
촉매Molybdenum oxideHCID 139765—
용매MethanolHCID 887—
생성물HCID 131724622HCID 13172462245.1%

반응 단계

1.44 g of sodium borohydride and 0.77 g of molybdenum oxide are added with stirring and under an inert atmosphere, at a temperature in the region of −5° C., to a solution of 2.05 g of methyl (3R,4R)-1-[3-(2,3,5-trifluorophenyl)prop-2-ynyl]-4-[3-hydroxyimino-3-(6-methoxyquinolin-4-yl)propyl]piperidine-3-carboxylate in 100 cm3 of methanol. After 5 hours at a temperature in the region of 20° C., the mixture is concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. The residue is purified by chromatography at atmospheric pressure on a column of silica gel (particle size 20-45μ; mass 30 g), elution being carried out with a dichloromethane/methanol/triethylamine (89/10/1 by volume) mixture. Fractions 3 to 5 (containing the purified product) are combined and then concentrated to dryness under the above conditions. 0.9 g of methyl (3R,4R)-1-[3-(2,3,5-trifluorophenyl)prop-2-ynyl]-4-[3-(R,S)-amino-3-(6-methoxyquinolin-4-yl)propyl]piperidine-3-carboxylate is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06806277B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-83d7dfc587c34a479d72ffac7d9dc5b1
출처 메모uspto-grants-2004_10