Triphosgene → Methyl 1,3-dihydro-4-methyl-2-oxo-thieno[3,4-d]imidazole-6-carboxylate

HRID 1598333

반응식

HRID 1598333 반응식
[NH2:1][C:2]1[C:6]([NH2:7])=[C:5]([CH3:8])[S:4][C:3]=1[C:9]([O:11][CH3:12])=[O:10].Cl[C:14](Cl)([O:16]C(=O)OC(Cl)(Cl)Cl)Cl>CN(C)C=O.ClCCl>[CH3:8][C:5]1[S:4][C:3]([C:9]([O:11][CH3:12])=[O:10])=[C:2]2[C:6]=1[NH:7][C:14](=[O:16])[NH:1]2

참가 물질

5

실험 절차

Methyl 3,4-diamino-5-methylthiophene-2-carboxylate (3.0 g) was dissolved in a mixture of N,N-dimethyl formamide (5 ml) and dichloromethane (15 ml). To the solution was added triphosgene (2.4 g) in portions. The mixture was stirred for two days at room temperature, and precipitates were collected by filtration, washed with dichloromethane and dried. Resultant white powder (2.4 g) was suspended in N,N-dimethylformamide (25 ml). To the suspension was added sodium hydride (60% in oil; 0.55 g), and the mixture was stirred for three days at room temperature. The solvent was evaporated under reduced pressure. To the residue was added 2N-HCl. Resulting precipitates were collected by filtration, washed with water, ether and methanol successively, followed by drying to afford the title compound (82 g, 53%) as pale brown powder.

후처리

  1. customprecipitates
  2. filtrationwere collected by filtration
  3. washwashed with dichloromethane
  4. customdried
  5. additionTo the suspension was added sodium hydride (60% in oil; 0.55 g)
  6. stirringthe mixture was stirred for three days at room temperature
  7. customThe solvent was evaporated under reduced pressure
  8. additionTo the residue was added 2N-HCl
  9. customResulting
  10. customprecipitates
  11. filtrationwere collected by filtration
  12. washwashed with water, ether and methanol successively
  13. customby drying

출처 및 근거

ORD 기록
ord-d1f8bbd3082843679aac7401c460d216
출처 데이터셋
uspto-grants-1998_04
특허 번호
US05736555

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