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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117901Generated: October 30, 2026

Tetrahydrofuran → HCID 91524016, compound

https://huagongshe.com/reaction/2117901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantTert-butyl (4-{2-[2-(acetylamino)-5-({[4-(methylthio)benzyl]amino}carbonyl)-1,3-thiazol-4-yl]ethyl}phenyl)carbamateHCID 86595599—
SolventWaterHCID 962—
ProductHCID 91524016HCID 91524016—

Reaction Steps

Potassium peroxymonosulfate (264 mg) was suspended in water (1 ml) and THF (1 ml), and then tert-butyl(4-{2-[2-(acetylamino)-5-({[4-(methylthio)benzyl]amino}carbonyl)-1,3-thiazol-4-yl]ethyl}phenyl)carbamate (155 mg) in THF (2 ml) was added dropwise to the suspension at 0° C. The reaction mixture was stirred at r.t. for an hour, and then water was added to the suspension. The solution was extracted with AcOEt (twice). The combined organic layer was washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo to give tert-butyl (4-{2-[2-(acetylamino)-5-({[4-(methylsulfonyl)benzyl]amino}carbonyl)-1,3-thiazol-4-yl]ethyl}phenyl)carbamate (140.6 mg) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-891219b531544b0e91dfae3da48d2df1
Source noteuspto-grants-2008_10