Triethylamine → 3-(2-Chlorophenyl)-2-(2-ethylcarbamoylethyl)-5,7-dimethyl-4-oxo-3,4-dihydroquinazoline-6-carboxylic Acid Ethyl Ester

HRID 1039365노트

반응식

HRID 1039365 반응식
[CH2:1]([O:3][C:4](=[O:26])[C:5]1[C:13]([CH3:14])=[CH:12][C:11]([NH:15][C:16](=O)[CH2:17][CH2:18][C:19]([O:21]CC)=O)=[C:7]([C:8]([OH:10])=O)[C:6]=1[CH3:25])[CH3:2].C(OC(=O)[C:31]1[C:39](C)=[CH:38][C:37]([NH2:41])=[C:33](C(O)=O)[C:32]=1C)C.[CH2:44]([N:46](CC)CC)[CH3:45].C(C(CC(Cl)=O)C([Cl:56])=O)C>ClCCl>[CH2:1]([O:3][C:4]([C:5]1[C:6]([CH3:25])=[C:7]2[C:11](=[CH:12][C:13]=1[CH3:14])[N:15]=[C:16]([CH2:17][CH2:18][C:19](=[O:21])[NH:46][CH2:44][CH3:45])[N:41]([C:37]1[CH:38]=[CH:39][CH:31]=[CH:32][C:33]=1[Cl:56])[C:8]2=[O:10])=[O:26])[CH3:2]

참가 물질

6

실험 절차

4-(3-Ethoxycarbonylpropionylamino)-2,6-dimethylisophthalic acid 1-ethyl ester: A stirred solution of 4-amino-2,6-dimethylisophthalic acid 1-ethyl ester (0.3 g, 1.26 mmol) and triethylamine (0.355 mL, 2.55 mmol) in dichloromethane (15 mL) at 0° C. is treated with ethyl succinyl chloride (0.199 mL, 1.39 mmol), and the reaction mixture is allowed to warm to room temperature overnight. The reaction mixture is washed with 1 M hydrochloric acid, back-washed with brine and dried over anhydrous MgSO4. The solvent is removed under reduced pressure to afford the title compound, which is used without further purification.

후처리

  1. washThe reaction mixture is washed with 1 M hydrochloric acid
  2. washback-washed with brine
  3. dry with materialdried over anhydrous MgSO4
  4. customThe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-597a5eed3804470c967de9592dc81776
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08552015B2

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