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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024913Generated: October 29, 2026

tert-Butyl 4-sulfamoylpiperazine-1-carboxylate → tert-butyl 4-{[(2-[(2,3-difluorobenzyl)thio]-6-{(1R)-1-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethoxy}pyrimidin-4-yl)amino]sulfonyl}piperazine-1-carboxylate

https://huagongshe.com/reaction/1024913

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-sulfamoylpiperazine-1-carboxylateHCID 53628347—
ReactantHCID 86619881HCID 86619881—
Producttert-butyl 4-{[(2-[(2,3-difluorobenzyl)thio]-6-{(1R)-1-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethoxy}pyrimidin-4-yl)amino]sulfonyl}piperazine-1-carboxylateHCID 53628363—

Reaction Steps

The subtitle compound was prepared from 1,1-dimethylethyl 4-sulfamoylpiperazine-1-carboxylate (the product of example 15, step i), 0.26 g) and 4-chloro-2-[(2,3-difluorobenzyl)thio]-6-{(1R)-1-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethoxy}pyrimidine (the product of Example 47, step i) (0.21 g) according to the procedure outlined in Example 1, step iv). Yield: 0.28 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722883B2
Source datasetuspto-grants-2014_05
ORD IDord-791c700b34364b69959e5bb3a35d0784
Source noteuspto-grants-2014_05