HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 86600475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86600474 | HCID 86600474 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86600475 | HCID 86600475 | 81% |
Reaction Steps
To a solution of 2-(benzyloxyamino-methyl)-4H-benzo[1,4]thiazin-3-one (2.96 mmol) in 15 mL of formic acid at 0° C., acetic anhydride is added (15.1 mmol) and the reaction is stirred at room temperature overnight. The mixture is diluted with EtOAc and washed with water followed by brine and NaHCO3. Purification by column chromatography (hexane/EtOAc) gives N-benzyloxy-N-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-ylmethyl)-formamide. Yield: 81%. MS: (ES+): 329.2 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253164B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-cbc9fd7bcfaa42338f4c62ef0b18bb14 |
| Source note | uspto-grants-2007_08 |