Triethylamine → 1-[5-(3-Cyano-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-3-[2-(5-ethyl-oxazol-2-yl)-ethyl]-urea
반응식
[C:1]([C:3]1[CH:4]=[C:5]([C:13]2[S:17][C:16]([NH:18][C:19]([N:21]3[CH:25]=[CH:24]N=C3)=[O:20])=[N:15][C:14]=2[CH3:26])[CH:6]=[CH:7][C:8]=1[S:9]([CH3:12])(=[O:11])=[O:10])#[N:2].[CH2:27]([C:29]1[O:33][C:32](CCN)=[N:31][CH:30]=1)[CH3:28].C(N(CC)CC)C>CN(C=O)C>[C:1]([C:3]1[CH:4]=[C:5]([C:13]2[S:17][C:16]([NH:18][C:19]([NH:21][CH2:25][CH2:24][C:32]3[O:33][C:29]([CH2:27][CH3:28])=[CH:30][N:31]=3)=[O:20])=[N:15][C:14]=2[CH3:26])[CH:6]=[CH:7][C:8]=1[S:9]([CH3:12])(=[O:11])=[O:10])#[N:2]참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 70 °C
실험 절차
To a stirred solution of imidazole-1-carboxylic acid [5-(3-cyano-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-amide (Intermediate BD) (0.05 g, 1.29 mmol) in DMF (1.5 ml) under an inert atmosphere is added 2-(5-ethyl-oxazol-2-yl)-ethylamine (Amine) (0.018 g, 1.29 mmol) followed by triethylamine (0.02 ml, 0.14 mmol). The reaction mixture is heated to 70° C. for 2.5 hours and then allowed to cool to room temperature. The solvent is removed in vacuo and the resulting crude residue is dissolved in THF and passed through a 0.5 g polymer supported isocyanate resin (pre-washed with THE). The solution is concentrated in vacuo and the crude residue is dissolved in DCM and washed with water, brine, dried over MgSO4 and concentrated in vacuo again. Triturating with ether affords the titled compound as a yellow solid.
후처리
- temperatureto cool to room temperature
- customThe solvent is removed in vacuo
- dissolutionthe resulting crude residue is dissolved in THF
- washpre-washed with THE)
- concentrationThe solution is concentrated in vacuo
- dissolutionthe crude residue is dissolved in DCM
- washwashed with water, brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo again
- customTriturating with ether
출처 및 근거
- ORD 기록
- ord-7849fa5456544017b5f8fba858f6346b
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07902375B2
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