HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22414427, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl orthopropionate | HCID 66995 | — |
| Reactant | HCID 22414364 | HCID 22414364 | — |
| Product | HCID 22414427 | HCID 22414427 | — |
Reaction Steps
A solution of 6.00 g of 2-amino-N-methyl-α-(3-thienyl)benzeneethanamine and 10 ml of triethyl orthopropionate, was treated with 8 ml of glacial acetic acid. After refluxing for eight hours, the volatile components were removed at 70° C. on a rotary evaporator. The residual oil was decanted into an ice-water mixture and basified with 10% sodium hydroxide solution. The aqueous mixture was extracted with dichloromethane and the organic phase was dried over anhydrous magnesium sulfate, filtered, and concentrated to provide 4,5-dihydro-2-ethyl-3-methyl-4-(3-thienyl)-3H-1,3-benzodiazepine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292760 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-b49e90b4bc9c4be99a6566b013fe8435 |
| Source note | uspto-grants-1994_03 |