HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271623Generated: October 31, 2026
1-Butanesulfonyl chloride → HCID 59834685, compound
https://huagongshe.com/reaction/271623
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Butanesulfonyl chloride | HCID 75430 | — |
| Reactant | HCID 59834656 | HCID 59834656 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59834685 | HCID 59834685 | 72% |
Reaction Steps
To a solution of 200 mg (0.59 mmoles) of 7-(2,2-dimethyl-propyl)-6-(2,6-dioxo-piperazin-1-ylmethyl)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile in 4 ml of pyridine, 184 mg (1.2 mmoles) of 1-butanesulfonylchloride is added at 0° C. The reaction mixture is allowed to warm to ambient temperature and stirred for 2 hours and the mixture is concentrated under reduced pressure. The obtained crude powder is dissolved in CH2Cl2, and the CH7Cl2 layer is washed with 1N aqueous HCl, brine, and then dried over MgSO4. The CH2Cl2 layer is concentrated under reduced pressure to give colorless powder, which is washed with ether to give 195 mg of desred 6-[4-(Butane-1-sulfonyl)-2,6-dioxo-piperazin-1-ylmethyl]-7-(2,2-dimethyl-propyl)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile in 72% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452886B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-84b8c39fe78642de9ae87a9c80ace4b9 |
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| Source note | uspto-grants-2008_11 |
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