5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

Base Information

Chemical Name:5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one
CAS No.:2894-52-2
Molecular Formula:C15H11ClN2O
Molecular Weight:270.718
Hs Code.:
DSSTox Substance ID:DTXSID20569361
Nikkaji Number:J433.061G
Mol file:2894-52-2.mol

Synonyms:2894-52-2;2H-1,4-Benzodiazepin-2-one, 5-(4-chlorophenyl)-1,3-dihydro-;SCHEMBL11543658;DTXSID20569361;5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one;AKOS004910818;AKOS032963749;Z1352548229

Suppliers and Price of 5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:270.0559907
Heavy Atom Count:19
Complexity:374

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(=O)NC2=CC=CC=C2C(=N1)C3=CC=C(C=C3)Cl

Technology Process of 5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

There total 6 articles about 5-(4-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 106-39-8
bromochlorobenzene

: 2894-52-2
5-(4-Chloro-phenyl)-1,3-dihydro-benzo[e][1,4]diazepin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 1) Mg 2) 2N HCl / 1) Et₂O, reflux, 30 min 2) Et₂O, reflux, 1 h

2: 98 percent / aq. 20percent Na₂CO₃ / diethyl ether; H₂O / 1 h / Ambient temperature

3: NH₃ / CH₂Cl₂ / 3 h / Heating

4: ethanol / 3 h / Heating

With hydrogenchloride; ammonia; sodium carbonate; magnesium; In diethyl ether; ethanol; dichloromethane; water;
DOI:10.1002/jhet.5570280704

Reference yield:

: 2894-51-1
2-amino-4'-chlorobenzophenone

: 2894-52-2
5-(4-Chloro-phenyl)-1,3-dihydro-benzo[e][1,4]diazepin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / aq. 20percent Na₂CO₃ / diethyl ether; H₂O / 1 h / Ambient temperature

2: NH₃ / CH₂Cl₂ / 3 h / Heating

3: ethanol / 3 h / Heating

With ammonia; sodium carbonate; In diethyl ether; ethanol; dichloromethane; water;
DOI:10.1002/jhet.5570280704

Reference yield:

: 138366-02-6
2-bromo-2'-(4-chlorobenzoyl)acetanilide

: 2894-52-2
5-(4-Chloro-phenyl)-1,3-dihydro-benzo[e][1,4]diazepin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: NH₃ / CH₂Cl₂ / 3 h / Heating

2: ethanol / 3 h / Heating

With ammonia; In ethanol; dichloromethane;
DOI:10.1002/jhet.5570280704