HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441257Generated: October 30, 2026
Dimethyl Sulfoxide → 1-formylmethyl-5-{4-[2-(4-methylphenyl)benzoylamino]benzoyl}-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one
https://huagongshe.com/reaction/441257
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22405269 | HCID 22405269 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-formylmethyl-5-{4-[2-(4-methylphenyl)benzoylamino]benzoyl}-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one | HCID 22405266 | 75.5% |
Reaction Steps
To a solution of oxalyl chloride (0.134 ml) in dichloromethane (10 ml) was added dimethyl sulfoxide (0.109 ml) at -78° C. and the mixture was stirred at the same temperature. After 10 minutes, 1-(2-hydroxyethyl) -5-{4-[2-(4-methylphenyl)benzoylamino]benzoyl}-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (400 mg) in dichloromethane (10 ml) was added dropwise at -78° C. and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added triethylamine (0.537 ml) and the mixture was allowed to ambient temperature. The solution was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated in vacuo to give 1-formylmethyl-5-{4-[2-(4-methylphenyl)benzoylamino]benzoyl}-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (301 mg) as an unstable oil. The oil was used for next step without further purification.
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-bcb89b0f601a4395b784ee5eabf0942a |
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| Source note | uspto-grants-1996_05 |
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