1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one

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1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one Basic information
Product Name:1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one
Synonyms:1,2,3,5-tetrahydro-1,5-benzodiazepin-4-one;2H-1,5-Benzodiazepin-2-one, 1,3,4,5-tetrahydro-;2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-2-one - [T28673]
CAS:5755-07-7
MF:C9H10N2O
MW:162.19
EINECS:
Product Categories:Aromatics;Heterocycles
Mol File:5755-07-7.mol
1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one Structure
1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one Chemical Properties
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
pka14.80±0.20(Predicted)
Safety Information
HS Code 2933998090
MSDS Information
1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one Usage And Synthesis
UsesA 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
1,3,4,5-Tetrahydro-2H-1,5-benzodiazepin-2-one Preparation Products And Raw materials
Raw materialso-Phenylenediamine-->methyl 3-((2-aminophenyl)amino)propanoate-->Acrylic acid-->Methanol-->Sodium
Preparation Products2,3,4,5-Tetrahydro-1H-benzo[b][1,4]diazepine
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