N-(4-(3-(3,4-dihydro-2H-pyran-2-yl)pyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine → (+/-)-N-(4-(3-(Tetrahydro-2H-pyran-2-YL)pyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amine
반응식
[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][CH:2]1[C:7]1[C:8]([O:13][C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:21]3[S:22][C:23]4[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=4[N:25]=3)=[CH:16][CH:15]=2)=[N:9][CH:10]=[CH:11][CH:12]=1>[Pd].C(O)C>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[C:7]1[C:8]([O:13][C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:21]3[S:22][C:23]4[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=4[N:25]=3)=[CH:16][CH:15]=2)=[N:9][CH:10]=[CH:11][CH:12]=1참가 물질
4
실험 절차
A mixture of N-(4-(3-(3,4-dihydro-2H-pyran-2-yl)pyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine (357 mg, 0.889 mmol) and palladium on carbon, wet (95 mg, 0.089 mmol) in ethanol (0.15M) was placed under an atmosphere of hydrogen (g) and stirred at room temperature. After the starting material was completely consumed, the mixture was filtered through a cake of celite, washed with MeOH & THF and filtrate was concentrated to dryness. The residue was purified by silica gel chromatography to give the desired product as a racemic mixture. MS (ESI, pos. ion) m/z: 404.0 (M+1). IC50 (uM) +++++.
후처리
- customAfter the starting material was completely consumed
- filtrationthe mixture was filtered through a cake of celite
- washwashed with MeOH & THF and filtrate
- concentrationwas concentrated to dryness
- customThe residue was purified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-257d504199d54a16b5e849cbc37230f6
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08759532B2
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