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5755-07-7

5755-07-7 Structure

5755-07-7 Structure
IdentificationBack Directory
[Name]

1,3,4,5-TETRAHYDRO-2H-1,5-BENZODIAZEPIN-2-ONE
[CAS]

5755-07-7
[Synonyms]

1,2,3,5-tetrahydro-1,5-benzodiazepin-4-one
2H-1,5-Benzodiazepin-2-one, 1,3,4,5-tetrahydro-
[Molecular Formula]

C9H10N2O
[MDL Number]

MFCD00612448
[MOL File]

5755-07-7.mol
[Molecular Weight]

162.19
Chemical PropertiesBack Directory
[Melting point ]

140.5-141.5 °C
[Boiling point ]

376.1±31.0 °C(Predicted)
[density ]

1.137±0.06 g/cm3(Predicted)
[storage temp. ]

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

14.80±0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335-H412
[Precautionary statements ]

P261-P273-P305+P351+P338
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

A tetrahydrobenzodiazepine derivative as arginine vasopressin antagonist.
[Synthesis]

methyl 3-((2-aminophenyl)amino)propanoate

1270914-58-3

1,3,4,5-TETRAHYDRO-2H-1,5-BENZODIAZEPIN-2-ONE

5755-07-7

The general procedure for the synthesis of 1,3,4,5-tetrahydro-benzo[b][1,4]diazepin-2-one from the compound (CAS: 1270914-58-3) is as follows: Step 3: Synthesis of 4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one 1. methanol (1.8 g, 77.2 mmol) was added in batches to methanol (50 mL) at 0 °C and the mixture was stirred for 1 hour. 2. the above mixture was added dropwise to a solution of methyl 3-((2-aminophenyl)amino)propionate (9.4 g, 48.2 mmol) in methanol (150 mL), keeping the temperature at 0 °C. the mixture was then stirred for 1 h. The mixture was then added to the methanol (50 mL) by dropwise addition. 3. After completion of the dropwise addition, the reaction mixture was stirred at room temperature overnight. 4. The reaction mixture was concentrated and the residue was purified by CombiFlash fast column chromatography (eluent: petroleum ether/ethyl acetate = 5:1) to afford 4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one as a yellow solid (3.9 g, 50% yield). Product Characterization: - LRMS (M + H)+: m/z 161 - 1H NMR (300 MHz, CD3OD): δ 2.61 (t, J = 6.0 Hz, 2H), 3.62 (t, J = 6.0 Hz, 2H), 6.76-6.86 (m, 2H), 6.90-6.99 (m, 2H).

[References]

[1] Patent: WO2012/151512, 2012, A2. Location in patent: Page/Page column 113-114
[2] ACS Medicinal Chemistry Letters, 2016, vol. 7, # 2, p. 145 - 150
Spectrum DetailBack Directory
[Spectrum Detail]

1,3,4,5-TETRAHYDRO-2H-1,5-BENZODIAZEPIN-2-ONE(5755-07-7)1HNMR
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