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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352376생성일: 2026년 10월 24일

Potassium Carbonate → (R)-1-tert-butylcarbonylmethyl-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/ko/reaction/352376

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-ChloropinacoloneHCID 83572—
반응물(R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 12043264—
촉매Potassium IodideHCID 4875—
촉매Tetrabutylammonium BromideHCID 74236—
용매Dimethyl SulfoxideHCID 679—
생성물(R)-1-tert-butylcarbonylmethyl-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 1204326599.8%

반응 단계

To a solution of 50 g of (R)-(−)-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine in 200 ml of dimethylsulfoxide were added 28.1 g of 1-chloropinacolone, 28.8 g of potassium carbonate (powder), 1.15 g of potassium iodide and 1.35 g of tetrabutylammonium bromide. The mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into ice water. The precipitate thus formed was collected by filtration with suction, washed with water and then dried, whereby 63.5 g of the title compound was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06747022B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-71aa540e1d8e46a180281fff0427b79a
출처 메모uspto-grants-2004_06