HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 8-Bromo-6-methyl-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 8-Bromo-6-methyl-3,4-dihydro-2h-1,4-benzoxazine | HCID 22557245 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Bromo-6-methyl-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid benzyl ester | HCID 20765681 | 96% |
Reaction Steps
A solution of benzyl chloroformate (1.32 g, 0.008 mol) in dichloromethane (20 mL) was added dropwise under nitrogen to an ice-cold solution of 8-bromo-6-methyl-3,4-dihydro-2H-benzo[1,4]oxazine (1.78 g, 0.007 mol) and pyridine (1.06 g, 0.013 mol) in dichlormethane (40 mL). After 1 hour at ambient temperature, a 10% aqueous HCl solution was added. The layers were separated and the organic phase was washed with water (50 mL×2), dried (Na2SO4) and concentrated to give 8-bromo-6-methyl-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid benzyl ester as a colorless oil (2.34 g, 96%) which was used in the step 2 without purification. Synthesis of 8-(4-tert-butoxycarbonyl-piperazin-1-yl)-6-chloro-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867204B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-96446da3632c4dfd8ca8ace08115ef2b |
| Source note | uspto-grants-2005_03 |