Methylamine → HCID 68893041, 화합물

HRID 1453834노트

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HRID 1453834 반응식
[CH2:1]([O:8][C:9]1[C:10]([C:28]([O:30]C)=O)=[N:11][N:12]2[CH2:17][CH:16]([CH3:18])[N:15]([CH2:19][C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=3)[C:14](=[O:27])[C:13]=12)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:32][NH2:33]>>[CH2:1]([O:8][C:9]1[C:10]([C:28]([NH:33][CH3:32])=[O:30])=[N:11][N:12]2[CH2:17][CH:16]([CH3:18])[N:15]([CH2:19][C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=3)[C:14](=[O:27])[C:13]=12)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

3

실험 절차

The title compound was prepared from methyl 3-benzyloxy-5-(4-fluorobenzyl)-6-methyl-4-oxo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-2-carboxylate using a procedure similar to that described in Example 5, Step 3, except that methylamine (2M in MeOH) was used in place of 4-fluorobenzylamine, and the reaction was heated to reflux overnight. The solvent was removed in vacuo, and the material was used without purification. ES MS (M+1)=423.

후처리

  1. temperaturethe reaction was heated
  2. temperatureto reflux overnight
  3. customThe solvent was removed in vacuo
  4. customthe material was used without purification

출처 및 근거

ORD 기록
ord-447598cb27e04c0ea778e977fcb18abc
출처 데이터셋
uspto-grants-2009_01
특허 번호
US07476666B2

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