HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 131717915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 54284901 | HCID 54284901 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131717915 | HCID 131717915 | — |
Reaction Steps
A solution of 1,1-dimethylethyl [3-[[2-(8-chloro-10,11-dihydrodibenz[b,f][1,4]-oxazepin-10-yl)-2oxoethyl]amino]-3-oxopropyl]carbamate (8.1 grams), glacial acetic acid (50 mL), and 6.95M HCl in dioxane (27 mL) was stirred at room temperature for 20 minutes. The reaction was evaporated in vacuo, and the residue was co-evaporated in vacuo twice with ethanol (3A; 170 mL each time). The resulting foam was crystallized from ethyl acetate/ethanol and dried in vacuo at 56° C. The yield of the title compound was 5.79 grams (85%). Analysis calculated for C18H26ClN3O3S×HCl: C, 54.56; H, 4.83;N, 10.60; Cl, 17.89. Found: C, 54.30; H, 4.79; N, 10.49; Cl, 16.77. DSC: 216°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382578 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-4488a585a73545a3a81cefe1f76f150e |
| Source note | uspto-grants-1995_01 |