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

HRID 842711
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 842711
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
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Komponenten

4

Edukt 2

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

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 80711,2-DimethoxyethaneLösungsmittel

Versuchsvorschrift

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:

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-e4eec364c1a5477e91952c71dc66b658
Quelldatensatz
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06376499B1

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