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Hydrazine hydrate (1:1) → 3-amino-1H-indazole-6-carboxylic Acid

HRID 537140
ノート
印刷プレビュー

反応式

HRID 537140 の反応式
[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][C:4]=1F)#[N:2].O.[NH2:14][NH2:15]>C(O)CCC>[NH2:2][C:1]1[C:3]2[C:4](=[CH:5][C:6]([C:7]([OH:9])=[O:8])=[CH:10][CH:11]=2)[NH:15][N:14]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 27784684-Cyano-3-fluorobenzoic acid

生成物 1

HCID 116007623-amino-1H-indazole-6-carboxylic Acid収率 26.3%

試薬・触媒・溶媒 1

HCID 2631-Butanol溶媒

反応条件

温度
110 °C

実験手順

To a solution of 4-cyano-3-fluorobenzoic acid (500 mg, 3.0 mmol) in n-butanol (9 mL) was added hydrazine monohydrate (0.5 mL, 10 mmol). The reaction was heated to 110° C. overnight. The reaction was cooled to room temperature and the precipitate was collected by filtration. The solid was then dissolved in 1 N aqueous sodium hydroxide (2 mL) and extracted with ethyl acetate (2×). The aqueous layer was acidified to pH=4 with 1 N aqueous hydrochloric acid. The resulting precipitate was collected by filtration and dried under vacuum to provide the title compound (140 mg, 26%) as a red solid. +ESI (M+H) 178.2; 1H NMR (400 MHz, CD3OD, δ): 7.99-8.01 (m, 1H), 7.73 (dd, J=8.4, 0.8 Hz, 1H), 7.61 (dd, J=8.5, 1.3 Hz, 1H).

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. filtrationthe precipitate was collected by filtration
  3. dissolutionThe solid was then dissolved in 1 N aqueous sodium hydroxide (2 mL)
  4. extractionextracted with ethyl acetate (2×)
  5. filtrationThe resulting precipitate was collected by filtration
  6. customdried under vacuum

出典と根拠

ORDレコード
ord-d0a8a5ee381640d9bb735577ef00c641
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859773B2

反応ノート

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