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N-Methylpiperidine → N-methyl-N-methoxy-2-chloro-5-sulfamoylthiophene-3-carboxamide

HRID 1197434
ノート
印刷プレビュー

反応式

HRID 1197434 の反応式
[Cl:1][C:2]1[S:6][C:5]([S:7]([NH2:10])(=[O:9])=[O:8])=[CH:4][C:3]=1[C:11]([OH:13])=O.CN1CCCCC1.Cl.[CH3:22][NH:23][O:24][CH3:25].C([O-])(O)=O.[Na+]>CN(C=O)C>[CH3:22][N:23]([O:24][CH3:25])[C:11]([C:3]1[CH:4]=[C:5]([S:7](=[O:9])(=[O:8])[NH2:10])[S:6][C:2]=1[Cl:1])=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 12291N-MethylpiperidineHCID 81138Methanamine, N-methoxy-, hydrochloride (1:1)HCID 516892Sodium BicarbonateHCID 12014982-Chloro-5-sulfamoylthiophene-3-carboxylic acid

生成物 1

HCID 19106478N-methyl-N-methoxy-2-chloro-5-sulfamoylthiophene-3-carboxamide収率 40.4%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

1,1-Carbonyldiimidazole (7.70 g, 0.047 mol) was added portionwise to a solution of 5-chloro-4-carboxythiophene-2-sulfonamide (7.25 g, 0.03 mol) in DMF (60 mL). After two hours, N-methylpiperidine (6.0 mL, 0.05 mol) and N,O-dimethylhydroxylamine hydrochloride (5.2 g, 0.05 mol) were added to the reaction mixture. After an additional four hours at room temperature, the reaction mixture was poured into ice/water saturated with NaHCO3. The crude product was extracted into ethyl acetate, the extract was dried (anhydrous Na2SO4), filtered and evaporated. The crude residue was chromatographed on silica gel and eluted with 59% methanol/methylene chloride to give 3.45 g (40%) of white solid product, mp 223°-225° C.

後処理

  1. waitAfter an additional four hours at room temperature
  2. extractionThe crude product was extracted into ethyl acetate
  3. dry with materialthe extract was dried (anhydrous Na2SO4)
  4. filtrationfiltered
  5. customevaporated
  6. customThe crude residue was chromatographed on silica gel
  7. washeluted with 59% methanol/methylene chloride

出典と根拠

ORDレコード
ord-1cc4ccf734414bdb81426a48f463ec72
出典データセット
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05276025

反応ノート

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