3-(Pyrrolidin-1-ylmethyl)thiomorpholine → 4-(6-Methoxy-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride
반응식
[N:1]1([CH2:6][CH:7]2[CH2:12][S:11][CH2:10][CH2:9][NH:8]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:13][O:14][C:15]1[CH:23]=[C:22]2[C:18]([C:19](=[O:27])[CH2:20][CH:21]2[C:24]([Cl:26])=[O:25])=[CH:17][CH:16]=1>C(N(CC)CC)C>[ClH:26].[CH3:13][O:14][C:15]1[CH:23]=[C:22]2[C:18]([C:19](=[O:27])[CH2:20][CH:21]2[C:24]([N:8]2[CH2:9][CH2:10][S:11][CH2:12][CH:7]2[CH2:6][N:1]2[CH2:2][CH2:3][CH2:4][CH2:5]2)=[O:25])=[CH:17][CH:16]=1참가 물질
4
실험 절차
The procedure described in Example 24 was repeated, but using 0.97 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.39 ml of triethylamine and 1.23 g of 6-methoxy-3-oxoindan-1-carbonyl chloride, to afford 0.9 g of the title compound, melting at 225°-233° C.
출처 및 근거
- ORD 기록
- ord-968e0d4781df4ce4993cf2ea810f61e7
- 출처 데이터셋
- uspto-grants-1997_08
- 특허 번호
- US05656758
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