HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441218Generated: October 30, 2026
Dimethylformamide → HCID 22405260, compound
https://huagongshe.com/reaction/441218
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Methoxy-4-nitrobenzoic acid | HCID 78764 | — |
| Reactant | 2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-2-one | HCID 223771 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22405260 | HCID 22405260 | 93.2% |
Reaction Steps
To a solution of 3-methoxy-4-nitrobenzoic acid (800 mg) and catalytic amount of N,N-dimethylformamide in dichloromethane (8 ml) was added oxalyl chloride (0.7 ml) at 0° C. and the solution was stirred at ambient temperature for 30 minutes followed by the removal of solvents to give a crude acid chloride. To a solution of 1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (658 mg) and triethylamine (821 mg) in dichloromethane (4 ml) was added a solution of the above acid chloride in dichloromethane (4 ml) at ambient temperature and the mixture was stirred at ambient temperature for 1 hour. The resultant mixture was filtered and the solid was washed with water and diethyl ether to give 5-(3-methoxy-4-nitrobenzoyl)-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (1.29 g) as a colorless prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521170 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-4f336c2b673b4b43936ae87a46bff1d1 |
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| Source note | uspto-grants-1996_05 |
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