Triethylamine → HCID 70629129, 화합물
반응식
C[CH:2](Cl)[C:3]([NH:5][C:6]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:7]=1[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9])=[O:4].[CH2:22](N(CC)CC)C.Cl.[CH3:30][NH:31][C:32](=[O:37])[CH2:33][CH2:34][NH:35][CH3:36]>C1(C)C(C)=CC=CC=1.C(OCC)C>[ClH:20].[CH3:30][NH:31][C:32]([CH2:33][CH2:34][N:35]([CH3:36])[CH2:2][C:3]([N:5]([C:6]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:7]=1[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9])[CH3:22])=[O:4])=[O:37]참가 물질
실험 절차
A mixture of 16.1 g of 2-(methyl-chloroacetamido)-5-chlorobenzophenone, 10 g of triethylamine and 7.6 g of 3-methylaminopropionic acid methylamide hydrochloride in 500 ml of anhydrous xylene is heated to reflux for 12 hours whilst stirring. The triethylamine hydrochloride which has precipitated is filtered off with suction after cooling and, after extracting three times by shaking with water, the organic phase is dried over anhydrous potassium carbonate, filtered and evaporated in vacuo. The oily crude base thus obtained (18 g) is dissolved in 800 ml of anhydrous diethyl ether and filtered and 17.0 g of 2-(5-methylaminocarbonyl-N-methyl-3-methyl-3-aza-pentanamido)-5-chlorobenzophenone hydrochloride (77% of theory), with a melting point of 151°-153°, are obtained by passing dry hydrogen chloride into the solution.
후처리
- temperatureis heated
- temperatureto reflux for 12 hours
- customThe triethylamine hydrochloride which has precipitated
- filtrationis filtered off with suction
- temperatureafter cooling
- extractionafter extracting three times
- stirringby shaking with water
- dry with materialthe organic phase is dried over anhydrous potassium carbonate
- filtrationfiltered
- customevaporated in vacuo
- customThe oily crude base thus obtained (18 g)
- filtrationfiltered
출처 및 근거
- ORD 기록
- ord-bd83244f89ce4795a04a52b00703d9cb
- 출처 데이터셋
- uspto-grants-1978_02
- 특허 번호
- US04075409
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