HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Pyrrolidineethanamine → 4-(7-Chloro-4-quinazolinylamino)-N-[2-(1-pyrrolidinyl)ethyl]benzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Pyrrolidineethanamine | HCID 1344 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(7-Chloro-4-quinazolinylamino)benzenesulphonyl chloride hydrochloride | HCID 21273954 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(7-Chloro-4-quinazolinylamino)-N-[2-(1-pyrrolidinyl)ethyl]benzenesulphonamide | HCID 13537205 | 26.4% |
Reaction Steps
4-(7-Chloro-4-quinazolinylamino)benzene sulphonyl chloride, hydrochloride (3.5 g, 0.011 mole) was added portionwise to a well-stirred mixture of sodium carbonate (11.5 g) in water (120 ml) and N-(2-aminoethyl)-pyrrolidine (1.26 g, 0.01 mole) in chloroform (120 ml) at about 10° C. After 1 hour at room temperature, the mixture was filtered. The chloroform layer was separated, dried (MgSO4) and evaporated under reduced pressure to give a gum. Trituration from ethyl acetate gave a white solid (1.14 g) which could be crystallised from ethanol-water, m.p. 203°-204.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734510 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-14b7c0cdd9c441d28777a75233d06a97 |
| Source note | uspto-grants-1988_03 |