Diethyl Ether → benzyl N-[(3R)-2-thioxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl]carbamate
반응식
COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:10])=CC=1.O=[C:24]1[C@H:30]([NH:31][C:32](=[O:41])[O:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[CH2:29][CH2:28][C:27]2[CH:42]=[CH:43][CH:44]=[CH:45][C:26]=2[NH:25]1.CCOCC>O1CCCC1>[S:10]=[C:24]1[C@H:30]([NH:31][C:32](=[O:41])[O:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[CH2:29][CH2:28][C:27]2[CH:42]=[CH:43][CH:44]=[CH:45][C:26]=2[NH:25]1참가 물질
실험 절차
Add Lawesson's Reagent (12.25 g, 30.29 mmol) to a solution of benzyl N-[(3R)-2-oxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl]carbamate (9.4 g, 30.29 mmol) in tetrahydrofuran (470 mL) and stir the reaction under nitrogen for approximately 16 hours at ambient temperature. Remove the precipitate by filtration and discard it. Concentrate the filtrate under reduced pressure and dissolve the residue in ethyl acetate. Wash with water and brine, dry over sodium sulfate, and concentrate the organic layer under reduced pressure to give a thick, yellow oil. Add ether to the thick oil and scratch it to form a solid. Collect the solid by filtration and wash it with ether. Triturate the solid with ether and collect it by filtration to give the title compound (7.28 g, 74%) as a white solid: MS (m/z): 349 (M+23).
후처리
- customthe reaction under nitrogen for approximately 16 hours at ambient temperature
- customRemove the precipitate
- filtrationby filtration
- concentrationConcentrate the filtrate under reduced pressure
- dissolutiondissolve the residue in ethyl acetate
- washWash with water and brine
- dry with materialdry over sodium sulfate
- concentrationconcentrate the organic layer under reduced pressure
- customto give a thick, yellow oil
- customCollect the solid
- filtrationby filtration
- washwash it with ether
- customTriturate the solid with ether
- customcollect it
- filtrationby filtration
출처 및 근거
- ORD 기록
- ord-b4baf5bf2060485d99ca5d2d98a2e19e
- 출처 데이터셋
- uspto-grants-2012_10
- 특허 번호
- US08299061B2
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