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Cyanamide → 2-(4-Aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrile

HRID 1167822
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HRID 1167822 반응식
[NH2:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([N:11]=[C:12]=[S:13])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[N:14]#[C:15][NH2:16].C1CCN2[C:20](=[N:21]CCC2)[CH2:19]C1.BrCC#N>C(#N)C>[NH2:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12]2[S:13][C:19]([C:20]#[N:21])=[C:15]([NH2:16])[N:14]=2)=[CH:9][CH:10]=1)(=[O:4])=[O:3]
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참가 물질

6

반응물 4

HCID 9864CyanamideHCID 11534BromoacetonitrileHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene2회HCID 5213594-Isothiocyanatobenzenesulfonamide

생성물 1

HCID 229939182-(4-Aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrile수율 49.4%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

To a solution of 4-(aminosulfonyl)phenylisothiocyanate (1.12 g, 5.0 mmol) and cyanamide (0.23 g, 5.5 mmol) in acetonitrile (50 ml) was added DBU (0.83 g, 5.5 mmol), and the resulting mixture was stirred at room temperature for 60 minutes. To the reaction mixture was added bromo-acetonitrile (0.66 g, 5.5 mmol) followed by DBU (0.83 g, 5.5 mmol) 30 minutes afterward. The reaction mixture was stirred overnight at room temperature, the solvent was removed at the reduced pressure, and the residue was dissolved in EtOAc (200 ml). The EtOAc solution was washed with 0.1 N HCl (150 ml×3) and brine and dried with MgSO4 and concentrated. The residue was purified by silica gel chromatography (EtOAc) to provide 0.73 g (48%) of 2-(4-aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrile.

후처리

  1. stirringThe reaction mixture was stirred overnight at room temperature
  2. customthe solvent was removed at the reduced pressure
  3. dissolutionthe residue was dissolved in EtOAc (200 ml)
  4. washThe EtOAc solution was washed with 0.1 N HCl (150 ml×3) and brine
  5. dry with materialdried with MgSO4
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel chromatography (EtOAc)

출처 및 근거

ORD 기록
ord-a846c747fc21416ebcf8cc3c852d28d7
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06620828B2

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