HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 86738857, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 20503433 | HCID 20503433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86738857 | HCID 86738857 | — |
Reaction Steps
A mixture of the above 6-[[[1-acetyl-4-(1-methoxy-1-methylethoxy)2-pyrrolidinyl]carbonyl]amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid, 75 ml of acetonitrile, 5 ml of dimethylformamide, and 3.47 g (24.4 mmol) carbonyldiimidazole is heated at 42°-50° for 2/3 hours and is stirred for 2 hours at room temperature. The mixture is cooled with ice and stirred overnight at room temperature. The solution is concentrated to an oil and treated with tetrahydrofuran and ether, and the solid filtered to give 1.70 g of 6-[[[1-acetyl-4-(1-methoxy-1-methylethoxy)-2-pyrrolidinyl]carbonyl]amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid imidazolide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382089 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-e0731adc921b4fbab360cbed2dbf7ad7 |
| Source note | uspto-grants-1983_05 |