HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570052Generated: October 26, 2026
Dichloromethane → 4-(7-Chloro-4-quinazolinylamino)-N-(2-diethylaminoethyl) benzenesulphonamide
https://huagongshe.com/reaction/570052
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | Sulphonylchloride hydrochloride | HCID 19012189 | — |
| Reactant | 4-(7-Chloro-4-quinazolinylamino)benzenesulphonyl chloride hydrochloride | HCID 21273954 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(7-Chloro-4-quinazolinylamino)-N-(2-diethylaminoethyl) benzenesulphonamide | HCID 13537202 | — |
Reaction Steps
4-(7-Chloro-4-quinazolinylamino)benzenesulphonyl chloride hydrochloride (36.0 g obtainable from the title compound of Example 1) and methylene chloride (180 ml) were cooled under nitrogen to 5° C. N,N-Diethylethylenediamine (35.4 g) was then added at 5°-10° C. over 20 minutes to give a light yellow solution. The solution was stirred for 2 hours under nitrogen at 5° to 15° C. and then water (200 ml) was added. A white solid precipitated. The mixture was cooled to 10° C. and the solid was filtered off, washed with water (2×40 ml) and with chloroform (2×40 ml) and dried in an oven to give 279 g of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734510 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-2c47d22c3667487cbcd36e337f5372f8 |
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| Source note | uspto-grants-1988_03 |
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