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Ethyl cyanoacetate → 6-Amino-1-[(3-isopropylisoxazol-5-yl)methyl]-2-thioxo-2,3-dihydropyrimidin-4(1H)-one

HRID 912690
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HRID 912690 반응식
[CH:1]([C:4]1[CH:8]=[C:7]([CH2:9][NH:10][C:11]([NH2:13])=[S:12])[O:6][N:5]=1)([CH3:3])[CH3:2].[O-]CC.[Na+].[C:18]([CH2:20][C:21](OCC)=[O:22])#[N:19]>>[NH2:19][C:18]1[N:10]([CH2:9][C:7]2[O:6][N:5]=[C:4]([CH:1]([CH3:3])[CH3:2])[CH:8]=2)[C:11](=[S:12])[NH:13][C:21](=[O:22])[CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7764Ethyl cyanoacetateHCID 2723922Sodium ethoxideHCID 86631131HCID 86631131, 화합물

생성물 1

HCID 866311326-Amino-1-[(3-isopropylisoxazol-5-yl)methyl]-2-thioxo-2,3-dihydropyrimidin-4(1H)-one수율 14%

실험 절차

The title compound was prepared in accordance with the general method described in Example 12(b) by using 1-[(3-isopropylisoxazol-5-yl)methyl]thiourea (1.11 g, 5.55 mmol, obtained from Example 15(a)), sodium ethoxide (21% w/v, 5.4 mL, 16.7 mmol) and ethyl cyanoacetate (1.8 mL, 16.7 mmol) with the exception that the reaction time after completed addition was 2 h. This provided 0.20 g (14% yield) of the title compound.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe title compound was prepared in accordance with the general method
  2. additionaddition

출처 및 근거

ORD 기록
ord-a6e26bad7ce345a79ba657359e82bfda
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08026244B2

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