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239097-74-6

239097-74-6 Structure

239097-74-6 Structure
IdentificationBack Directory
[Name]

Benzo[d]isoxazol-5-ylaMine
[CAS]

239097-74-6
[Synonyms]

1,2-benzoxazol-5-amine
BENZO[D]ISOXAZOL-5-AMINE
1,2-benzisoxazol-5-amine
5-Aminobenzo[d]isoxazole
1,2-Benzoisoxazol-5-amine
Benzo[d]isoxazol-5-ylaMine
Benzo[d]isoxazol-5-ylamine(AK-64412)
[Molecular Formula]

C7H6N2O
[MDL Number]

MFCD13190363
[MOL File]

239097-74-6.mol
[Molecular Weight]

134.14
Chemical PropertiesBack Directory
[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
[pka]

2.67±0.10(Predicted)
[Appearance]

Light yellow to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H302-H335
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
Spectrum DetailBack Directory
[Spectrum Detail]

Benzo[d]isoxazol-5-ylaMine(239097-74-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-NITRO-1,2-BENZISOXAZOLE

39835-28-4

Benzo[d]isoxazol-5-ylaMine

239097-74-6

GENERAL STEPS: To a 12M HCl (0.5 mL) solution of SnCl4 (1.828 g, 7.02 mmol) under stirring was added 5-nitro-1,2-benzisoxazole (140 mg, 0.86 mmol) in a single addition at 0 °C. After a few minutes of reaction, a 12M HCl (0.5 mL) solution of SnCl2-2H2O (792 mg, 3.51 mmol) was added slowly and dropwise at 0 °C, followed by the addition of 12M HCl (1.0 mL). The reaction mixture was brought to room temperature and stirred continuously for 3 hours. Upon completion of the reaction, the reaction mixture was extracted with Et2O. The aqueous phase was adjusted to pH ~8 with saturated NaHCO3 solution and subsequently extracted with EtOAc. The organic phases were combined, dried with anhydrous Na2SO4, filtered and concentrated, and dried in vacuum to give 1,2-benzisoxazol-5-amine as a colorless solid (110 mg, 95% yield). The product was confirmed by 1H NMR (400 MHz, CDCl3): δ 8.54 (s, 1H), 7.42 (d, J=8.4 Hz, 1H), 6.94 (dd, J=8.4 Hz, 2.0 Hz, 1H), 6.91 (d, J=2.0 Hz, 1H). es-MS m/z: 135.1 [M+H]+. lc-MS analysis Shows purity of 90% (214 nm), retention time tR = 1.32 min.

[References]

[1] Patent: WO2016/73889, 2016, A1. Location in patent: Paragraph 00229
[2] Patent: WO2016/73895, 2016, A1. Location in patent: Paragraph 00286
[3] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 18, p. 6189 - 6196
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