ChemicalBook--->CAS DataBase List--->222036-66-0

222036-66-0

222036-66-0 Structure

222036-66-0 Structure
IdentificationBack Directory
[Name]

5-Aminoisoindolin-1-one
[CAS]

222036-66-0
[Synonyms]

5-aminoisoindolin-1-one
5-aMinoisoindoline-1-one
5-aMino-2,3-dihydro- Isoindol-1-one
5-amino-2,3-dihydro-1H-Isoindol-1-one
1H-Isoindol-1-one, 5-amino-2,3-dihydro
1H-Isoindol-1-one,5-amino-2,3-dihydro-(9CI)
5-Aminoisoindolin-1-one ISO 9001:2015 REACH
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C8H8N2O
[MDL Number]

MFCD10000828
[MOL File]

222036-66-0.mol
[Molecular Weight]

148.16
Chemical PropertiesBack Directory
[Melting point ]

197-199 °C(Solv: ethyl acetate (141-78-6))
[Boiling point ]

520.0±50.0 °C(Predicted)
[density ]

1.307±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

15.12±0.20(Predicted)
[color ]

Yellow
[InChI]

InChI=1S/C8H8N2O/c9-6-1-2-7-5(3-6)4-10-8(7)11/h1-3H,4,9H2,(H,10,11)
[InChIKey]

RGJCJWXNNDARPQ-UHFFFAOYSA-N
[SMILES]

C1(=O)C2=C(C=C(N)C=C2)CN1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

5-Aminoisoindolin-1-one is used in the synthesis of a novel potent glycoprotein IIb-IIIa (GP IIb-IIIa) receptor antagonist based on the isoindolone skeleton.
[Synthesis]

6-NITRO-ISOINDOLIN-1-ONE

110568-64-4

5-Aminoisoindolin-1-one

222036-66-0

General procedure for the synthesis of 5-amino-2,3-dihydroisoindol-1-one from 6-nitro-isoindolin-1-one: A mixture of 6-nitro-isoindolin-1-one (100 mg, 0.56 mmol), and reduced iron powder (314 mg, 5.6 mmol) was added to ethanol (2.0 mL) and concentrated hydrochloric acid (0.5 mL) and heated and refluxed for 2 hours. The completion of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, it was cooled to room temperature, the acid in the reaction solution was neutralized with a methanol solution saturated with ammonia (NH3), filtered through diatomaceous earth, the filtrates were washed with methanol, the filtrates were combined and the solvent was evaporated under reduced pressure to give 5-amino-2,3-dihydroisoindol-1-one (70.0 mg, 84% yield) as a white solid.

[References]

[1] Patent: CN103804358, 2016, B. Location in patent: Paragraph 0126
[2] Patent: WO2012/92880, 2012, A1. Location in patent: Page/Page column 57
[3] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 287
[4] Patent: WO2006/17443, 2006, A2. Location in patent: Page/Page column 154-155
[5] Patent: US2010/15141, 2010, A1. Location in patent: Page/Page column 26
Spectrum DetailBack Directory
[Spectrum Detail]

5-Aminoisoindolin-1-one(222036-66-0)1HNMR
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