HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980570Generated: October 27, 2026
4-Piperidino-6-quinazolinesulfonyl chloride → N-(4-aminobutyl)-4-piperidino-6-quinazolinesulfonamide
https://huagongshe.com/reaction/1980570
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Piperidino-6-quinazolinesulfonyl chloride | HCID 13044234 | — |
| Reactant | 1,4-Diaminobutene | HCID 73447540 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(4-aminobutyl)-4-piperidino-6-quinazolinesulfonamide | HCID 13044235 | 77.5% |
Reaction Steps
In 100 ml of chloroform was dissolved 4.4 g of 1,4-diaminobutene, and to the solution was added dropwise 50 ml of a chloroform solution containing 3.1 g of 4-piperidino-6-quinazolinesulfonyl chloride under cooling with ice. After the dropwise addition of the chloroform solution, the mixed solution was stirred at a temperature of 20° C. to 25° C. for two hours, and the reaction solution was extracted with a 10% aqueous hydrochloric acid solution. The chloroform layer was washed with water and dried with anhydrous potassium carbonate. Then chloroform was distilled from the chloroform layer, and the residue was separated by Prep LC/System 500 (Waters Associates, U.S.A.) [column: Prepack 500/C18 ; solvent: H2O/CH3CN=85/15 (volume ratio); flow rate: 100 ml/minute] to give 2.8 g of N-(4-aminobutyl)-4-piperidino-6-quinazolinesulfonamide [i.e. Compound(31)] as an oily substance in a yield of 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04510307 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-44eadc7e5f8c4e93b68d3b9da50cc8ae |
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| Source note | uspto-grants-1985_04 |
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