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Dichloromethane → HCID 23111116, 화합물

HRID 2100644
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HRID 2100644 반응식
ON1C2N=CC=CC=2N=N1.ClCCl.[Br:14][C:15]1[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=1[NH2:17].[CH2:22]([N:24]([CH2:32][CH2:33][CH2:34][C:35](O)=[O:36])[C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[CH:26]=1)[CH3:23]>C(OCC)(=O)C.C(N(CC)CC)C>[Br:14][C:15]1[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=1[NH:17][C:35](=[O:36])[CH2:34][CH2:33][CH2:32][N:24]([CH2:22][CH3:23])[C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6344DichloromethaneHCID 119922-BromoanilineHCID 181649HOAtHCID 231111194-(Ethyl-3-methylanilino)butyric acid

생성물 1

HCID 23111116HCID 23111116, 화합물

시약·촉매·용매 2

HCID 8471Triethylamine용매
HCID 8857
Ethyl Acetate
용매

실험 절차

1-Ethyl-3-(3-dimethylamindpropyl)carbodiimide hydrochloride (150 mg), 1-hydroxy-7-azabenzotriazole (106 mg), dichloromethane (2 ml), 2-bromoaniline (134 μl), and triethylamine (162 μl) were added to the compound (100 mg) obtained in Step 2, and the mixture was stirred at room temperature for 17 hours. The reaction mixture was diluted with ethyl acetate, washed with water, and dried over magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel chromatography (hexane-ethyl acetate) to give the title compound (56 mg).

후처리

  1. washwashed with water
  2. dry with materialdried over magnesium sulfate
  3. customThe solvent was evaporated
  4. customthe residue was purified by silica gel chromatography (hexane-ethyl acetate)

출처 및 근거

ORD 기록
ord-2f5c9c5060254705b98271e1ef7ff29e
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572815B2

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