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2-Bromoacetamide → 3-Amino-4,6-dimethylthieno(2,3-b)pyridine-2-carboxamide

HRID 488921
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인쇄 미리보기

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HRID 488921 반응식
Br[CH2:2][C:3]([NH2:5])=[O:4].[SH:6][C:7]1[N:14]=[C:13]([CH3:15])[CH:12]=[C:11]([CH3:16])[C:8]=1[C:9]#[N:10].C[O-].[Na+]>CO>[NH2:10][C:9]1[C:8]2[C:7](=[N:14][C:13]([CH3:15])=[CH:12][C:11]=2[CH3:16])[S:6][C:2]=1[C:3]([NH2:5])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 696322-BromoacetamideHCID 10942334Sodium MethoxideHCID 178425247HCID 178425247, 화합물

생성물 1

HCID 6135283-Amino-4,6-dimethylthieno(2,3-b)pyridine-2-carboxamide수율 80%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

α-Bromoacetamide (388 mg, 2.81 mmol) was added to a solution of 2-mercapto-4,6-dimethyl-nicotinonitrile (420 mg, 2.56 mmol) in MeOH (25 mL) at room temperature. This was followed by addition of sodium methoxide (1.76 mL, 25% NaOMe in MeOH, 7.7 mmol). The reaction mixture was heated to reflux. Heating at reflux was continued overnight, after which time the reaction mixture was cooled and filtered. The product was dried overnight providing 450 mg (80%) of the title compound, m.p. 238-40° C.

후처리

  1. temperatureThe reaction mixture was heated to reflux
  2. temperatureHeating
  3. temperatureat reflux
  4. temperatureafter which time the reaction mixture was cooled
  5. filtrationfiltered
  6. customThe product was dried overnight

출처 및 근거

ORD 기록
ord-1f2adbfdf41b4220ad40b94de5d3222a
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06974870B2

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