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Methane → N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide

HRID 867837
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HRID 867837 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([S:7]([NH2:10])(=[O:9])=[O:8])[CH:2]=1.C[Al](C)C.C.[CH3:16][C:17]1[CH:22]=[C:21]([CH3:23])[N:20]=[C:19]([NH:24][C:25](=O)[O:26]C)[N:18]=1>C(Cl)Cl.C(O)(=O)C>[CH3:16][C:17]1[CH:22]=[C:21]([CH3:23])[N:20]=[C:19]([NH:24][C:25]([NH:10][S:7]([C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)(=[O:9])=[O:8])=[O:26])[N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 297MethaneHCID 232710Pyridine-3-sulfonamideHCID 13278970Methyl (4,6-dimethylpyrimidin-2-yl)carbamateHCID 16682925Trimethylaluminum

생성물 1

HCID 13533294N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide

시약·촉매·용매 2

HCID 176Acetic Acid
용매
HCID 6344Dichloromethane용매

실험 절차

To a slurry of 3-pyridinesulfonamide (1 m mole) in methylene chloride is added 2 m mole of trimethylaluminum. Following methane evolution, the reaction mixture becomes homogeneous, whereupon 1 m mole of methyl (4,6-dimethylpyrimidin-2-yl)carbamate is added, and stirring is continued for 66 hours. Aqueous acetic acid is added and the product is extracted into methylene chloride. The solvent is evaporated and the product is isolated by trituration on chromatography.

후처리

  1. additionis added
  2. extractionthe product is extracted into methylene chloride
  3. customThe solvent is evaporated
  4. customthe product is isolated by trituration on chromatography

출처 및 근거

ORD 기록
ord-f2fdf6bce19d40c49b15db1c6293b280
출처 데이터셋
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04776878

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