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

HRID 842711
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HRID 842711 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 114578353-Amino-1,2-benzisoxazole-6-carbonitrileHCID 12423031(Dimethyl sulfide)trihydroboron

생성물 1

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

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

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:

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후처리

  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)

출처 및 근거

ORD 기록
ord-e4eec364c1a5477e91952c71dc66b658
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06376499B1

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