Methylamine → 2-Methylamino-N-(6-oxo-5,6-dihydro-phenanthridin-2-yl)-acetamide

HRID 880829노트

반응식

HRID 880829 반응식
Cl[CH2:2][C:3]([NH:5][C:6]1[CH:19]=[CH:18][C:17]2[NH:16][C:15](=[O:20])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8]=2[CH:7]=1)=[O:4].[CH3:21][NH2:22]>CN(C)C=O.C(O)C>[CH3:21][NH:22][CH2:2][C:3]([NH:5][C:6]1[CH:19]=[CH:18][C:17]2[NH:16][C:15](=[O:20])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8]=2[CH:7]=1)=[O:4]

참가 물질

5

반응물 2

HCID 6329MethylamineHCID 9814438N-(6-oxo-5,6-dihydro-phenanthridin-2-yl)-chloroacetamide

생성물 1

HCID 668198452-Methylamino-N-(6-oxo-5,6-dihydro-phenanthridin-2-yl)-acetamide

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6228Dimethylformamide용매

실험 절차

To a stirred suspension of 150 mg of 2-chloro-N-(6-oxo-5,6-dihydro-phenanthridin-2-yl)-acetamide (XV) (0.52 mmol) in N,N-dimethylformamide (1.4 mL), 9 mL of a 33% solution of methylamine in ethanol were added (mM). The reaction mixture was stirred at room temperature for 3 hours. The ethanol was then evaporated under reduced pressure and the mixture was diluted with diethyl ether and filtered. A light-yellow solid was then collected, washed with ether then with cold water and dried. The title compound was obtained in moderate yield (100 mg, 68%).

후처리

  1. additionwere added (mM)
  2. customThe ethanol was then evaporated under reduced pressure
  3. additionthe mixture was diluted with diethyl ether
  4. filtrationfiltered
  5. customA light-yellow solid was then collected
  6. washwashed with ether
  7. dry with materialwith cold water and dried

출처 및 근거

ORD 기록
ord-fbe0d5fe7ea740ddb8b71c5c53f2a7d8
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08993594B2

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