HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623025Generated: October 31, 2026
1,1'-Carbonyldiimidazole → HCID 23037390, compound
https://huagongshe.com/reaction/623025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1-Ethylpyrrolidin-3-amine | HCID 12861942 | — |
| Reactant | 2-(3-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid | HCID 14390454 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23037390 | HCID 23037390 | 59% |
Reaction Steps
A solution of 2-(3-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (5.0 g, 0.0174 mole), 1,1'-carbonyldiimidazole (2.82 g, 0.0174 mole) and anhydrous tetrahydrofuran (100 ml) was stirred at room temperature with a stream of nitrogen bubbling through it for 3 hours. The nitrogen flow was stopped and a solution of 1-ethyl-3-aminopyrrolidine (2.18 g, 0.0192 mole) in dry tetrahydrofuran (25 ml) was added. The solution was stirred at room temperature under nitrogen for 1 hour. The reaction mixture was concentrated in vacuo and the residue triturated in potassium bicarbonate solution (75 ml) and filtered. The filter cake was washed with water and recrystallized from isopropyl alcohol-isopropyl ether to give 2.25 g (28%) of beige solid, mp 154°-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04772600 |
|---|
| Source dataset | uspto-grants-1988_09 |
|---|
| ORD ID | ord-e038bc34f1b4446ab38bda768a8d140f |
|---|
| Source note | uspto-grants-1988_09 |
|---|