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

HRID 410233노트

반응식

HRID 410233 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]=1

참가 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

  1. customAfter the starting material was completely consumed
  2. filtrationthe mixture was filtered through a cake of celite
  3. washwashed with MeOH & THF and filtrate
  4. concentrationwas concentrated to dryness
  5. 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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