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3-Amino-1,2-benzisoxazole-6-carbonitrile → 3-Amino-1,2-benzisoxazole-6-methanamine

HRID 842711
ノート
印刷プレビュー

反応式

HRID 842711 の反応式
CSC.B.[NH2:5][C:6]1[C:10]2[CH:11]=[CH:12][C:13]([C:15]#[N:16])=[CH:14][C:9]=2[O:8][N:7]=1>COCCOC>[NH2:5][C:6]1[C:10]2[CH:11]=[CH:12][C:13]([CH2:15][NH2:16])=[CH:14][C:9]=2[O:8][N:7]=1
参加物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 114578353-Amino-1,2-benzisoxazole-6-carbonitrileHCID 12423031(Dimethyl sulfide)trihydroboron

生成物 1

HCID 220647313-Amino-1,2-benzisoxazole-6-methanamine

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane溶媒

実験手順

Borane methylsulfide complex (2 M in THF, 1.98 mL) was added to a stirred refluxing solution of 3-amino-6-cyano-1,2-benzisoxazole (210 mg, 1.32 mmol) in DME (10 mL). After 45 min excess methyl sulfide was evaporated and the reaction mixture was cooled and quenched with 1M HCl solution (10 mL). The mixture was stirred for 30 min and then was neutralised with sodium bicarbonate solution and concentrated to dryness. The residue was triturated with 5% methanol/chloroform, filtered and the filtrate evaporated in vacuo. The residue was purified by chromatography on silica (5% methanol, chloroform/ammonia) to give the title compound as a yellow solid:

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customAfter 45 min excess methyl sulfide was evaporated
  2. temperaturethe reaction mixture was cooled
  3. customquenched with 1M HCl solution (10 mL)
  4. concentrationconcentrated to dryness
  5. customThe residue was triturated with 5% methanol/chloroform
  6. filtrationfiltered
  7. customthe filtrate evaporated in vacuo
  8. customThe residue was purified by chromatography on silica (5% methanol, chloroform/ammonia)

出典と根拠

ORDレコード
ord-e4eec364c1a5477e91952c71dc66b658
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06376499B1

反応ノート

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