HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Ro 14-7437
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | ethyl alpha-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate | HCID 70542724 | — |
| Product | Ro 14-7437 | HCID 127597 | — |
Reaction Steps
4.1 g of ethyl α-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate are dissolved in 25 ml of ethyl acetate, treated with 3.1 ml (18.1 mmol) of N,N-dimethylformamide diethyl acetal and heated to boiling under reflux for 0.5 hour. After cooling, the separated material is filtered off under suction and recrystallised from ethanol. After chromatography of the mother liquor, there is obtained a second portion of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of the same purity; melting point 166°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04346030 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-3e3aa5f130f14bf1a33e3cd58dbcc0c4 |
| Source note | uspto-grants-1982_08 |