HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamidine monohydrochloride → HCID 13271777, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Butyl 8-chloro-1-phenyl-3H-2-benzazepine-5-carboxylate | HCID 13271771 | — |
| Reactant | Butyl 8-chloro-1-phenyl-5H-2-benzazepine-5-carboxylate | HCID 13271773 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13271777 | HCID 13271777 | — |
Reaction Steps
In one portion, 11.5 mL (49 mmol) of a 4.34 M methanol solution of sodium methoxide was added to a solution of 11.0 g (31 mmol) of a mixture of 8-chloro-1-phenyl-5H-2-benzazepine-5-carboxylic acid butyl ester and 8-chloro-1-phenyl-3H-2-benzazepine-5-carboxylic acid butyl ester and 5.7 g (60 mmol) of acetamidine hydrochloride in 200 mL of ethanol. The mixture was refluxed for 18 hr, cooled and poured into 800 mL of water. The resulting precipitate was collected by filtration and washed with ether to yield a yellow solid. Recrystallization from tetrahydrofuran gave off-white prisms, mp 155°-160°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04427589 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-c7125d6ff43d4451a86e2ebff6065e63 |
| Source note | uspto-grants-1984_01 |