반응식
Cl[C:2](Cl)([O:4]C(=O)OC(Cl)(Cl)Cl)Cl.[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([N:20]2[C:24](=[O:25])[C:23]3=[CH:26][C:27]([Cl:30])=[CH:28][CH:29]=[C:22]3[C:21]2=[O:31])=[C:16]([CH3:32])[CH:15]=1.[Cl:33][C:34]1[S:38][C:37]([CH2:39][NH2:40])=[CH:36][CH:35]=1>C(Cl)Cl.C(N(CC)C(C)C)C.CCN(C(C)C)C(C)C>[Cl:33][C:34]1[S:38][C:37]([CH2:39][NH:40][C:2]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([N:20]3[C:24](=[O:25])[C:23]4[CH:26]=[C:27]([Cl:30])[CH:28]=[CH:29][C:22]=4[C:21]3=[O:31])=[C:16]([CH3:32])[CH:15]=2)=[O:4])=[CH:36][CH:35]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 3
실험 절차
To a solution of triphosgene (22 mg, 0.074 mmol) in CH2Cl2 (1 mL) was added a suspension of N-(4-amino-2-methylphenyl)-4-chlorophthalimide (57 mg, 0.2 mmol) in CH2Cl2 (1.5 mL) and diethylisopropylamine (70 μL) dropwise over 10 min. The reaction mixture was stirred for 10 min, then a solution (5-chloro-2-thienyl)methylamine from step B (47 mg, 0.32 mmol) in CH2Cl2 (1 mL) and DIEA (35 μL) was added. The mixture was stirred at room temp for 17 hr, acidified and HPLC purified to give {[(5-chloro(2-thienyl))methyl]amino}-N-[4-(5-chloro-1,3-dioxobenzo[c]azolidin-2-yl)-3-methylphenyl]carboxamide (18 mg, 20%). ES-MS (M+H)+=460, 462 (Cl). 1H-NMR (DMSO-d6): δ 2.02 (s, 3H), 4.34-4.36 (d, 2H), 6.77-6.80 (t, 1H), 6.82-6.93 (2d, 2H), 7.14-7.16 (d, 1H), 7.29-7.32 (dd, 1H), 7.41 (d, 1H), 7.93 (ABq, 2H), 8.02 (s, 1H), 8.77 (s, 111).
후처리
- stirringThe mixture was stirred at room temp for 17 hr
- customHPLC purified
출처 및 근거
- ORD 기록
- ord-15fedfe23781411c9d8969224653e0a7
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08524721B2
연결된 노트
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