HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131717522, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | (4-mercaptophenyl) 3 (4-pyridyl) 6,7dihydro[5H]-pyrrolo[1,2-a]imidazole | HCID 135962046 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131717522 | HCID 131717522 | — |
Reaction Steps
To an ice bath cooled solution containing 1.0 g 3.4mmole) of 2-(4-mercaptophenyl)-3-(4-pyridyl)-6,7-dihydro-[5H]-pyrrolo[1,2-a]imidazole prepared as in Example 16 and 0.5 ml (3.6mmole) of triethylamine in 10 ml of methylene chloride is added 0.33 ml (3.5 mmole) of ethyl chloroformate. The reaction is allowed to warm to room temperature and stirred for several hours. Workup and chromatography in a manner analogous to that outlined in Example 18 affords the desired titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05145858 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-6bbb933d34944769a6d161874d8f34cb |
| Source note | uspto-grants-1992_09 |