HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroquinoline-4-carbonyl chloride → 2-Chloro-N-(1-cyclohexylpyrrolidin-3-yl)quinoline-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroquinoline-4-carbonyl chloride | HCID 75438 | — |
| Reactant | 1-Cyclohexylpyrrolidin-3-amine | HCID 3670074 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Chloro-N-(1-cyclohexylpyrrolidin-3-yl)quinoline-4-carboxamide | HCID 20355405 | — |
Reaction Steps
To 3.16 gm. (0.0195 mole) of 3-amino-1-cyclohexylpyrrolidine in 50 ml. of chloroform was added dropwise a solution of 3.5 gm. (0.015 mole) of 2-chloro-4-quinolinecarbonyl chloride in 50 ml. of chloroform. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate containing 10% isopropyl ether and dilute hydrochloric acid. The separated acid layer was made basic with dilute sodium hydroxide solution and extracted with chloroform. The chloroform solution was dried over sodium sulfate, concentrated and the residue recrystallized twice from isopropyl ether-ethyl acetate. The product (0.7 gm.; 13%) melted at 127°-219° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087428 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-ab02c6ffd09e4230abcdae91bc596b11 |
| Source note | uspto-grants-1978_05 |