Triethylamine → 5-isopropyl-1-methyl-1H-indazole-4-carboxylic acid indan-2-yl-(4-methyl-benzyl)-amide

HRID 857944노트

반응식

HRID 857944 반응식
[CH:1]([C:4]1[CH:12]=[CH:11][C:10]2[N:9]([CH3:13])[N:8]=[CH:7][C:6]=2[C:5]=1[C:14](Cl)=[O:15])([CH3:3])[CH3:2].[C:17]1(C)[CH:22]=[CH:21][C:20]([NH:23][CH:24]2[CH2:32][C:31]3[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=3)[CH2:25]2)=[CH:19][CH:18]=1.[CH2:34](N(CC)CC)[CH3:35]>C1COCC1.C(OCC)(=O)C>[CH2:32]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[CH2:25][CH:24]1[N:23]([CH2:20][C:19]1[CH:18]=[CH:17][C:22]([CH3:21])=[CH:35][CH:34]=1)[C:14]([C:5]1[C:6]2[CH:7]=[N:8][N:9]([CH3:13])[C:10]=2[CH:11]=[CH:12][C:4]=1[CH:1]([CH3:3])[CH3:2])=[O:15]

참가 물질

6

실험 절차

5-Isopropyl-1-methyl-1H-indazole-4-Carbonyl chloride (0.618 mmol, 1.0 eq) (30) in 5 ml of THF is added to a solution of (4-tolyl)-indan-2-yl-amine (147 mg, 0.618 mmol) (31) in 5 ml of tetrahydrofuran containing 250 mg of triethylamine at 0° C. The resulting mixture is stirred at room temperature overnight, diluted with 20 ml of ethyl acetate, washed with water and brine, and dried over sodium sulfate. Concentration and purification by silica gel chromatography affords 168 mg of 5-isopropyl-1-methyl-1H-indazole-4-Carboxylic acid indan-2-yl-(4-methyl-benzyl)-amide (32). 1H NMR (400 MHz, CDCl3) 7.89 (1H, s), 7.42˜6.92 (10H, m), 4.95 (1H, d J=15.2 Hz), 4.66 (1H, d, J=15.2 Hz), 4.551 (1H, m), 4.05 (3H, s), 3.26˜2.73 (5H, m), 2.36 (3H, s), 1.34 (6H, dd, J=1.6, 6.8 Hz). MS (+VE) m/z 438 (M++1).

후처리

  1. washwashed with water and brine
  2. dry with materialdried over sodium sulfate
  3. concentrationConcentration and purification by silica gel chromatography

출처 및 근거

ORD 기록
ord-ca0ce7eabc1648fd810900dda34250a1
출처 데이터셋
uspto-grants-2006_12
특허 번호
US07148225B2

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