HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-[5-(Dibenz[b,f][1,4]oxazepin-10(11H)-ylcarbonyl)-2-pyridinyl]-5-fluoro-2-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine | HCID 648933 | — |
| Reactant | 6-(5-Fluoro-2-methylbenzoyl)aminopyridine-3-carbonyl chloride | HCID 15508250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[5-(Dibenz[b,f][1,4]oxazepin-10(11H)-ylcarbonyl)-2-pyridinyl]-5-fluoro-2-methylbenzamide | HCID 9846717 | — |
Reaction Steps
As described for Example 46, 10,11-dihydrodibenz[b,f][1,4]oxazepine is reacted in dichloromethane with 2-[(2-methyl-5-fluorobenzoyl)amino]-5-pyridinylcarbonyl chloride in the presence of N,N-diisopropylethylamine to give the product as crystals. m.p. 180° C.-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849735 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-48c9381bc53340ddb584b7e4c8490108 |
| Source note | uspto-grants-1998_12 |