HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611533Generated: October 30, 2026
Water → N-[4-(4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzenesulphonamide
https://huagongshe.com/reaction/611533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(4-Aminophenyl)-4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidine | HCID 19597487 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-(4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzenesulphonamide | HCID 19597404 | — |
Reaction Steps
Benzenesulphonyl chloride (0.27 g) in dichloromethane (5 ml) was added dropwise with stirring to a solution of 5-(4-aminophenyl)-4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidine (0.40 g) and triethylamine (155 mg) in dichloromethane (15 ml) at 0° C. under nitrogen. The mixture was stirred at 0° C. for one hour and then warmed to ambient temperature and stirred at this temperature for 18 hours. Water (20 ml) was added and the mixture was extracted with dichloromethane. The combined organic layers were washed with sodium bicarbonate, dried, filtered and evaporated to give N-[4-(4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzenesulphonamide
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06001839 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-ec17fdec137f4630aa6d22648b38799b |
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| Source note | uspto-grants-1999_12 |
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