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Ammonia → 1-phenyl-1H-1,2,3-triazole-5-carboxamide

HRID 1506624
ノート
印刷プレビュー

反応式

HRID 1506624 の反応式
[C:1]1([N:7]2[C:11]([C:12]([OH:14])=O)=[CH:10][N:9]=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C[N:16]1CCOCC1.ClC(OCC(C)C)=O.N.O1CCOCC1>COCCOC>[C:1]1([N:7]2[C:11]([C:12]([NH2:16])=[O:14])=[CH:10][N:9]=[N:8]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 222AmmoniaHCID 79724-MethylmorpholineHCID 312751,4-DioxaneHCID 62365Isobutyl chloroformateHCID 28017501-phenyl-1H-1,2,3-triazole-5-carboxylic acid

生成物 1

HCID 184741521-phenyl-1H-1,2,3-triazole-5-carboxamide

試薬・触媒・溶媒 1

HCID 8071
1,2-Dimethoxyethane
溶媒

実験手順

To a solution of 1-phenyl-1H-1,2,3-triazole-5-carboxylic acid (1.0 g, 5.6 mmol) and 4-methylmorpholine (0.57 g, 5.6 mmol) in 1,2-dimethoxyethane (5 mL), isobutyl chloroformate (0.77, 5.6 mmol) was added to the mixture. After 30 minutes, ammonia in dioxane (16.8 mL, 8.4 mmol) was added to the reaction. Then it was stirred overnight. The solvent was removed and dissolved in 50 mL of ethyl acetate. The organic layer was washed with brine twice. The organic layer was dried with Na2SO4, filtered and concentrated and used without further purification. MS (m/z) 189 [M+H]+.

後処理

  1. customThe solvent was removed
  2. dissolutiondissolved in 50 mL of ethyl acetate
  3. washThe organic layer was washed with brine twice
  4. dry with materialThe organic layer was dried with Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customused without further purification

出典と根拠

ORDレコード
ord-e267bd35a98e4a4aac73c3a79838a321
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09220710B2

反応ノート

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