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Lithium Hydroxide → 3-cyano-1H-indazole-6-carboxylic acid

HRID 537135
ノート
印刷プレビュー

反応式

HRID 537135 の反応式
[C:1]([C:3]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([O:14]C)=[O:13])=[CH:9][CH:10]=2)[NH:5][N:4]=1)#[N:2].[OH-].[Li+]>CO.O1CCCC1>[C:1]([C:3]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([OH:14])=[O:13])=[CH:9][CH:10]=2)[NH:5][N:4]=1)#[N:2]
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

5

反応物 2

HCID 3939Lithium HydroxideHCID 67491426methyl 3-cyano-1H-indazole-6-carboxylate

生成物 1

HCID 674913803-cyano-1H-indazole-6-carboxylic acid収率 37%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
50 °C

実験手順

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

To a solution of methyl 3-cyano-1H-indazole-6-carboxylate (1.47 g, 7.31 mmol) in methanol (36 mL) and tetrahydrofuran (20 mL) was added 2 N aqueous lithium hydroxide (16 mL, 32 mmol). The reaction was heated to 50° C. for 72 hours. The reaction was cooled to room temperature and concentrated. The residue was diluted with water and the pH was adjusted to 4 with 1 N aqueous hydrochloric acid. The resulting precipitate was filtered off, rinsed with water, and dried under vacuum to provide the title compound (500 mg, 37%) as a tan solid. +ESI (M+H) 188.2.

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. concentrationconcentrated
  3. additionThe residue was diluted with water
  4. filtrationThe resulting precipitate was filtered off
  5. washrinsed with water
  6. customdried under vacuum

出典と根拠

ORDレコード
ord-036e77bb3b434f6f8858f348eec4b53d
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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