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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356116생성일: 2026년 10월 25일

Diethyl dithiophosphate, potassium salt → (5S)-1-azabicyclo[3.3.0]octane-3-carbothioamide

https://huagongshe.com/reaction/356116

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl dithiophosphate, potassium saltHCID 1385274—
반응물(5S)-1-azabicyclo[3.3.0]octane-3-carbonitrileHCID 67758565—
용매Hydrochloric AcidHCID 313—
용매Ethyl AcetateHCID 8857—
생성물(5S)-1-azabicyclo[3.3.0]octane-3-carbothioamideHCID 86753315—

반응 단계

In 100 ml of 4N solution of hydrogen chloride in ethyl acetate, 5.10 g of a diastereomer mixture of (5S)-1-azabicyclo[3.3.0]octane-3-carbonitrile was dissolved. Then, 7 g of O,O-diethyl dithiophosphate was added, followed by stirring at room temperature for 16 hours. After the solvent was evaporated, the residue was washed with ethyl acetate, followed by drying under reduce pressure, whereby (5S)-1-azabicyclo[3.3.0]octane-3-carbothioamide was obtained. The resulting product was dissolved in 150 ml of isopropanol, 6.3 g of 2-bromo-1-indanone and 3.7 g of calcium carbonate were added, and the mixture was heated under reflux for 5 hours. After cooling, the insoluble matter was removed by filtration and the solvent was evaporated. To the resulting residue, ethyl acetate and 1N hydrochloric acid were added. The aqueous layer was separated, and neutralized with sodium bicarbonate, followed by extraction with chloroform. The extract was dried over anhydrous sodium sulfate. The solvent was evaporated, and the resulting residue was subjected to preparative medium-pressure column chromatography, whereby 0.32 g of a (3R,5S) form compound (Example 63A) and 0.18 g of a (3S,5S) form compound (Example 63B) of 3-(8H-indeno[1,2-d]thiazol-2-yl)-1-azabicyclo[3.3.0]octane was obtained from the fraction eluted with chloroform-methanol-aqueous ammonia (200:10:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834499
출처 데이터셋uspto-grants-1998_11
ORD IDord-71640c78bfd2473284d2fab28adb89d6
출처 메모uspto-grants-1998_11