Methanol → 5-[4,6-Difluoro-5-(1-methyl-1H-indol-5-yl)-1H-benzoimidazol-2-yloxy]-2-methyl-benzoic acid

HRID 1945298노트

반응식

HRID 1945298 반응식
C[O:2][C:3](=[O:33])[C:4]1[CH:9]=[C:8]([O:10][C:11]2[NH:15][C:14]3[CH:16]=[C:17]([F:31])[C:18]([C:21]4[CH:22]=[C:23]5[C:27](=[CH:28][CH:29]=4)[N:26]([CH3:30])[CH:25]=[CH:24]5)=[C:19]([F:20])[C:13]=3[N:12]=2)[CH:7]=[CH:6][C:5]=1[CH3:32].CO.O.[OH-].[Na+]>C1COCC1>[F:20][C:19]1[C:13]2[N:12]=[C:11]([O:10][C:8]3[CH:7]=[CH:6][C:5]([CH3:32])=[C:4]([CH:9]=3)[C:3]([OH:33])=[O:2])[NH:15][C:14]=2[CH:16]=[C:17]([F:31])[C:18]=1[C:21]1[CH:22]=[C:23]2[C:27](=[CH:28][CH:29]=1)[N:26]([CH3:30])[CH:25]=[CH:24]2

참가 물질

6

실험 절차

A solution of 5-[4,6-difluoro-5-(1-methyl-1H-indol-5-yl)-1H-benzoimidazol-2-yloxy]-2-methyl-benzoic acid methyl ester (655 mg, 1.464 mmol) in THF:MeOH:H2O (7 mL) was treated with sodium hydroxide (1N, 3 mL) at room temperature. After 3 h, another 3 mL of sodium hydroxide (1N) was added and stirred at room temperature for another 1.5 h, and at 50° C. for another 1.5 h. The cooled reaction solution was concentrated on a rotavapor and the resulting aqueous solution was neutralized with 1N hydrogen chloride (6 mL), and the resulting white solid was collected through filtration (washed with water) and dried under high vacuum to give the desired product as a white solid. LC-MS: calculated for C24H17F2N3O3 434.41, observed m/e 434.6 (M+H)+ (Rt 1.52 min). 1H NMR (300 MHz, DMSO-d6): δ 7.78-7.15 (m, 8H), 6.45 (d, J=3.3 Hz, 1H), 3.81 (s, 3H), 2.53 (s, 3H).

후처리

  1. waitat 50° C. for another 1.5 h
  2. customThe cooled reaction solution
  3. concentrationwas concentrated on a rotavapor
  4. filtrationthe resulting white solid was collected through filtration (washed with water)
  5. customdried under high vacuum

출처 및 근거

ORD 기록
ord-1ff539ae3f3e4265b0fe5de0c7da32d9
출처 데이터셋
uspto-grants-2013_03
특허 번호
US08394969B2

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