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Triethylamine → 2-Butyl-4-chloro-1-[[1-(2-cyanophenyl)-1H-indol-4-yl]methyl]-1H-imidazole-5-carboxylic acid, 5-indanyl ester

HRID 1492492
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HRID 1492492 반응식
[CH2:1]([C:5]1[N:6]([CH2:14][C:15]2[CH:23]=[CH:22][CH:21]=[C:20]3[C:16]=2[CH:17]=[CH:18][N:19]3[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:30]#[N:31])[C:7]([C:11]([OH:13])=[O:12])=[C:8]([Cl:10])[N:9]=1)[CH2:2][CH2:3][CH3:4].[CH2:32]1[C:40]2[C:35](=[CH:36][C:37](O)=[CH:38][CH:39]=2)[CH2:34][CH2:33]1.CNC1C=CC=C(NC)N=1.C(N(CC)CC)C.Cl.CN(C)CCCN=C=NCC>ClCCl>[CH2:1]([C:5]1[N:6]([CH2:14][C:15]2[CH:23]=[CH:22][CH:21]=[C:20]3[C:16]=2[CH:17]=[CH:18][N:19]3[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:30]#[N:31])[C:7]([C:11]([O:13][C:37]2[CH:36]=[C:35]3[C:40](=[CH:39][CH:38]=2)[CH2:32][CH2:33][CH2:34]3)=[O:12])=[C:8]([Cl:10])[N:9]=1)[CH2:2][CH2:3][CH3:4]
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참가 물질

7

반응물 5

HCID 8471TriethylamineHCID 151185-IndanolHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 111943672-N,6-N-dimethylpyridine-2,6-diamineHCID 189503772-butyl-4-chloro-1-[[1-(2-cyanophenyl)-1H-indol-4-yl]methyl]-1H-imidazole-5-carboxylic acid

생성물 1

HCID 57248162
2-Butyl-4-chloro-1-[[1-(2-cyanophenyl)-1H-indol-4-yl]methyl]-1H-imidazole-5-carboxylic acid, 5-indanyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a mixture containing 2-butyl-4-chloro-1-[[1-(2-cyanophenyl)-1H-indol-4-yl]methyl]-1H-imidazole-5-carboxylic acid (903 mg, 2.03 mmol, prepared as described in part C of Example 9), 5-indanol (307 mg, 2.29mmol), 2,6-dimethylaminopyridine (50.8 mg, 0.416 mmol) and triethylamine (0.377 mL, 2.70 mmol) in 9 mL of dichloromethane cooled in an ice bath was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (519 mg, 2.70 mmol). The stoppered reaction mixture was allowed to warm to ambient temperature overnight, then diluted with methylene chloride and rinsed with water and saturated aqueous sodium chloride solution. The organic extract was dried over anhydrous magnesium sulfate and concentrated in vacuo to give 1.83 g of crude product. Flash chromatography on 75 g of silica gel eluted with 8:2, hexanes:ethyl acetate gave 1.03 g of the title A compound.

후처리

  1. temperaturecooled in an ice bath
  2. customThe stoppered reaction mixture
  3. washrinsed with water and saturated aqueous sodium chloride solution
  4. extractionThe organic extract
  5. dry with materialwas dried over anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customto give 1.83 g of crude product
  8. washFlash chromatography on 75 g of silica gel eluted with 8:2, hexanes
  9. customethyl acetate gave 1.03 g of the title A compound

출처 및 근거

ORD 기록
ord-de562a164a004bcc8b6cb31711508a92
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374615

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