Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959384Generated: November 1, 2026

Ethanesulfonyl chloride → Tert-butyl N-tert-butoxycarbonyl-5-(4-(ethylsulfonyl)piperazin-1-yl)-3-((trimethylsilyl)ethynyl)pyrazin-2-ylcarbamate

https://huagongshe.com/reaction/1959384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66744546HCID 66744546—
SolventDimethylformamideHCID 6228—
ProductTert-butyl N-tert-butoxycarbonyl-5-(4-(ethylsulfonyl)piperazin-1-yl)-3-((trimethylsilyl)ethynyl)pyrazin-2-ylcarbamateHCID 66745624109.3%

Reaction Steps

Ethanesulfonyl chloride (147.0 mg, 108.3 μL, 1.143 mmol) was added slowly to a stirred solution of tert-butyl N-tert-butoxycarbonyl-5-(piperazin-1-yl)-3-((trimethylsilyl)ethynyl)pyrazin-2-ylcarbamate (494 mg, 1.039 mmol) and DIPEA (161.2 mg, 217.3 μL, 1.247 mmol) in DMF (5 mL) at ambient temperature. The reaction was allowed to stir for 5 minutes and then partitioned between EtOAc/water. The aqueous layer was extracted with EtOAc (3×) and the combined organics washed with brine, dried (MgSO4), filtered and concentrated to give the product as a terracotta oil (645 mg, quantitative yield). MS (ES+) 590.05

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410112B2
Source datasetuspto-grants-2013_04
ORD IDord-666c29755a78445ca37d103c6af8676b
Source noteuspto-grants-2013_04