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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271623Generated: October 31, 2026

1-Butanesulfonyl chloride → HCID 59834685, compound

https://huagongshe.com/reaction/271623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Butanesulfonyl chlorideHCID 75430—
ReactantHCID 59834656HCID 59834656—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 59834685HCID 5983468572%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452886B2
Source datasetuspto-grants-2008_11
ORD IDord-84b8c39fe78642de9ae87a9c80ace4b9
Source noteuspto-grants-2008_11