반응식
C(N(CC)CC)C.Cl.[Cl:9][C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[NH:15][CH:14]=[C:13]2[CH2:19][CH2:20][NH2:21].Cl[C:23](=[O:29])[C:24]([O:26]CC)=[O:25].[OH-].[Na+].Cl>ClCCl>[Cl:9][C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[NH:15][CH:14]=[C:13]2[CH2:19][CH2:20][NH:21][C:23](=[O:29])[C:24]([OH:26])=[O:25]참가 물질
실험 절차
Triethylamine (2.28 mL; 16.22 mmol) was added to the mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (1.53 g; 6.49 mmol) and ethyl 2-chloro-2-oxoacetate (0.815 mL; 7.14 mmol) in dichloromethane (50 mL) at 0° C. After addition, the mixture was stirred at room temperature for 30 minutes and washed with an aqueous solution of sodium carbonate, dried over magnesium sulfate, and concentrated under reduced pressure. Ethanol (2 mL) and water (7.5 mL) were added to the resulting residue, followed by a 2M solution of sodium hydroxide (9.5 mL, 19 mmol). The mixture was stirred at room temperature for 20 minutes and the pH of the solution was adjusted to 1 by addition of a 6N hydrochloric acid. The precipitate was collected, and was dissolved in ethyl acetate. The ethyl acetate layer was dried over magnesium sulfate and was evaporated to dryness to give 1.36 g (81%) of 2-(2-(5-chloro-1H-indol-3-yl)ethylamino)-2-oxoacetic acid as a yellowish solid.
후처리
- additionAfter addition
- washwashed with an aqueous solution of sodium carbonate
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- additionEthanol (2 mL) and water (7.5 mL) were added to the resulting residue
- stirringThe mixture was stirred at room temperature for 20 minutes
- customThe precipitate was collected
- dissolutionwas dissolved in ethyl acetate
- dry with materialThe ethyl acetate layer was dried over magnesium sulfate
- customwas evaporated to dryness
출처 및 근거
- ORD 기록
- ord-a7d993b520b6444581f0b2e0f57d7396
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09434722B2
연결된 노트
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