HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Diethylethylenediamine → 4-(6-Chloro-4-quinazolinylamino)-N-(2-diethylaminoethyl)benzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | 4-(6-Chloro-4-quinazolinylamino)benzenesulphonic acid | HCID 13537209 | — |
| Reactant | Sulphonylchloride hydrochloride | HCID 19012189 | — |
| Product | 4-(6-Chloro-4-quinazolinylamino)-N-(2-diethylaminoethyl)benzenesulphonamide | HCID 13537210 | — |
Reaction Steps
The sulphonyl chloride hydrochloride derivative of the sulphonic acid or part (a) was used to sulphonylate N,N-diethylethylenediamine using a similar procedure to Example 8. The crude product obtained after evaporation of solvent from the chloroform layer was a brown solid which was purified by column chromatography (basic alumina: 1% ethanol/chloroform) to give a creamy white solid. Recrystallisation from ethanol/water gave the title compound hemihydrate, m.p. 110°-113° C. Analysis: Calculated for C20H24ClNSO2S.1/2H2O C, 54.2%; H, 5.69%; N, 15.8%. Found C, 54.3%; H, 5.64%; N, 16.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808715 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-dde01f6918cb40a986e690b44be734ec |
| Source note | uspto-grants-1989_02 |