HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457691Generated: November 3, 2026
Water → N-[4-(Dibenz[b,f][1,4]oxazepin-10(11H)-ylcarbonyl)-phenyl][1,1'-biphenyl]-2-carboxamide
https://huagongshe.com/reaction/1457691
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine | HCID 648933 | — |
| Reactant | 4-(2-Phenylbenzoylamino)-benzoylchloride | HCID 11450501 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-(Dibenz[b,f][1,4]oxazepin-10(11H)-ylcarbonyl)-phenyl][1,1'-biphenyl]-2-carboxamide | HCID 22099982 | 131.1% |
Reaction Steps
To a mixture of 0.197 g of 10,11-dihydrodibenz[b,f][1,4]oxazepine and 0.402 g of 4-[([1,1'-biphenyl]-2-carbonyl)amino]benzoyl chloride in 5 ml of dichloromethane (cooled in ice bath) is added dropwise 0.154 g of N,N-diisopropylethylamine in 2 ml of dichloromethane. The mixture is stirred at room temperature under argon for 2 hours. The mixture is poured into water and the organic layer separated. The organic extract is washed with 2N Na2CO3, water, brine and dried (Na2SO4). The solution is filtered through a thin pad of hydrous magnesium silicate and the filter cake washed with dichloromethane. The filtrate is concentrated to dryness to give 0.65 g of solid. The solid is purified by thick layer chromatography on silica gel with hexane-ethyl acetate (2:1) as solvent to give 0.110 g of a glass, m.p. 107° C.-122° C. Anal. Found: C, 80.8; H, 4.9; N,6.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849735 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-e375ac38b0774716ba52f5797d944af0 |
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| Source note | uspto-grants-1998_12 |
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