Dichloromethane → N-(3-(4-chloro-1-methyl-1H-pyrazol-5-yl)-4-hydroxyphenyl)-5-methylisoxazole-3-carboxamide

HRID 1685945노트

반응식

HRID 1685945 반응식
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]([OH:9])=O)[CH:3]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[NH2:43][C:44]1[CH:49]=[CH:48][C:47]([OH:50])=[C:46]([C:51]2[N:55]([CH3:56])[N:54]=[CH:53][CH:52]=2)[CH:45]=1.C(Cl)[Cl:58]>>[Cl:58][C:52]1[CH:53]=[N:54][N:55]([CH3:56])[C:51]=1[C:46]1[CH:45]=[C:44]([NH:43][C:7]([C:4]2[CH:3]=[C:2]([CH3:1])[O:6][N:5]=2)=[O:9])[CH:49]=[CH:48][C:47]=1[OH:50]

참가 물질

6

실험 절차

To a solution of 5-methylisoxazole-3-carboxylic acid (284.0 mg, 2236.0 μmol) dissolved in DCM(10.0 mL) was added HATU (1020.0 mg, 2683.0 μmol) followed by DIEA (586 μl, 3353 μmol). The solution was stirred at room temperature for 5 minutes. 4-amino-2-(1-methyl-1H-pyrazol-5-yl)phenol (500.00 mg, 2236 μmol) was added and the reaction mixture was stirred at 25° C. for 15 hours. The reaction mixture was subjected to purification by column chromatography (ethyl acetate:hexane 50:50) to afford the title compound as an off-white solid in 59.0% yield. LCMS m/z=333.2 (M+H), 1H NMR (400 MHz, DMSO-d6) δ ppm 2.69 (s, 3 H), 3.66 (s, 3 H), 6.64 (s, 1 H), 7.00 (d, J=8.84 Hz, 1 H), 7.61 (s, 1 H), 7.64 (d, J=2.53 Hz, 1 H), 7.73 (dd, J=8.84, 2.53 Hz, 1 H), 10.04 (s, 1 H), 10.60 (s, 1 H).

후처리

  1. stirringthe reaction mixture was stirred at 25° C. for 15 hours
  2. customThe reaction mixture was subjected to purification by column chromatography (ethyl acetate:hexane 50:50)

출처 및 근거

ORD 기록
ord-46542986dbd84d66a1c6ec7c5c465f5d
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08148417B2

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