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Methylamine → 2-amino-5-(benzyloxy)-N,1-dimethyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide

HRID 1409590
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인쇄 미리보기

반응식

HRID 1409590 반응식
[NH2:1][C:2]1[N:3]([CH3:21])[C:4](=[O:20])[C:5]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[C:6]([C:8]([O:10]C)=O)[N:7]=1.[CH3:22][NH2:23].C1COCC1>>[CH3:22][NH:23][C:8]([C:6]1[N:7]=[C:2]([NH2:1])[N:3]([CH3:21])[C:4](=[O:20])[C:5]=1[O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6329MethylamineHCID 8028TetrahydrofuranHCID 86710288Methyl 2-amino-5-(benzyloxy)-1-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate

생성물 1

HCID 867102892-amino-5-(benzyloxy)-N,1-dimethyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide수율 100%

반응 조건

온도
140 °C

실험 절차

To a mixture of methyl 2-amino-5-(benzyloxy)-1-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate (0.907 g, 3.14 mmol, Eq: 1.00), methylamine 2M in THF (12 ml, 24.0 mmol) was added. The mixture was heated in a microwave oven at 140° C. for 2 h. The crude reaction mixture was concentrated in vacuo to give the title product as an off-white solid (0.90 g; 100%). LCMS: m/z=289 (MH+).

후처리

  1. additionwas added
  2. customThe crude reaction mixture
  3. concentrationwas concentrated in vacuo

출처 및 근거

ORD 기록
ord-56c5994e6fb04cb68cbe748ff9e55e9f
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921388B2

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