HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 14648560, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 67931189 | HCID 67931189 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14648560 | HCID 14648560 | — |
Reaction Steps
In 300 ml of methanol is dissolved 8 g of ethyl trans-3-amino-4-oxo-2-(2-thienyl)-2,3,4,5-tetrahydro-1,5 -benzothiazepine-5-acetate, and ammonia gas is under ice-cooling blown into the solution until being saturated with ammonia gas. The reaction temperature is slowly elevated to room temperature, and the mixture is left standing for one day. Thereafter, the reaction mixture is concentrated under reduced pressure. Isopropyl alcohol is added to the obtained residue to crystallize. The crystals are collected by filtration to give 7 g of trans-3 amino-4-oxo-2-(2-thienyl)-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetamide, m.p. 207°-210° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05055464 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-6be1b2f7df0548a784a3e962d3e33f39 |
| Source note | uspto-grants-1991_10 |