3-Amino-1,2-benzisoxazole

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CAS:36216-80-5
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  • CAS:36216-80-5
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3-Amino-1,2-benzisoxazole Basic information
Product Name:3-Amino-1,2-benzisoxazole
Synonyms:OTAVA-BB BB7119710108;AKOS BBS-00002920;1,2-BENZISOXAZOL-3-AMINE;IFLAB-BB F1935-0009;BENZO[D]ISOXAZOL-3-YLAMINE;3-Amino-1,2-benzisoxazole;3-Amino-1,2-benzisoxazole 97%;1,2-Benzisoxazol-3-amine ,97%
CAS:36216-80-5
MF:C7H6N2O
MW:134.14
EINECS:
Product Categories:Amines;Fused Ring Systems
Mol File:36216-80-5.mol
3-Amino-1,2-benzisoxazole Structure
3-Amino-1,2-benzisoxazole Chemical Properties
Melting point 110 °C
Boiling point 311.6±15.0 °C(Predicted)
density 1.317±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka2.04±0.30(Predicted)
color White to Off-White
Stability:Hygroscopic
CAS DataBase Reference36216-80-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-36-25
Safety Statements 26-36/37/39-37/39-45
HazardClass IRRITANT
HS Code 29349990
MSDS Information
3-Amino-1,2-benzisoxazole Usage And Synthesis
Chemical PropertiesWhite to light brown solid
Uses1,2-Benzisoxazol-3-amine is a useful reagent for the preparation of benzisoxazole sulfonamides useful in treatment of diseases
Synthesis Reference(s)Journal of Heterocyclic Chemistry, 26, p. 1293, 1989 DOI: 10.1002/jhet.5570260515
Synthesis
2-Fluorobenzonitrile

394-47-8

3-Amino-1,2-benzisoxazole

36216-80-5

General procedure for the synthesis of 1,2-benzisoxazol-3-amine from 2-fluorobenzonitrile: (1) Synthesis of 1,2-benzisoxazol-3-amine: potassium tert-butoxide (14.9 g, 133 mmol) was added to a solution of N,N-dimethylformamide (150 ml) containing acetohydroxamic acid (10.0 g, 133 mmol), and stirred for 30 min at room temperature. Subsequently 2-fluorobenzonitrile (18.0 g, 133 mmol) was added and the reaction continued to be stirred at room temperature for 5 hours. After completion of the reaction, the mixture was poured into water and extracted with ethyl acetate. The organic phases were combined, washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure and the residue was recrystallized from hexane to give 4.80 g (27.0% yield) of the target product 1,2-benzisoxazol-3-amine as a solid. The product was characterized by 1H-NMR (CDCl3): δ 4.43 (2H, br s), 7.23-7.28 (1H, m), 7.43 (1H, d, J = 9.3Hz), 7.50-7.56 (2H, m).

References[1] Patent: EP1813606, 2007, A1. Location in patent: Page/Page column 24
[2] Journal of Organic Chemistry, 2000, vol. 65, # 10, p. 2924 - 2932
[3] Journal of Heterocyclic Chemistry, 1989, vol. 26, p. 1293 - 1298
[4] Patent: EP2460799, 2012, A1
[5] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 18, p. 6157 - 6165
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