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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941621Generated: October 29, 2026

Chlorotrimethylsilane → HCID 57030967, compound

https://huagongshe.com/reaction/1941621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantChlorosulfamic acidHCID 24499—
Reactant1-Pyrrolidinecarboxylic acid, 2-(aminomethyl)-4-mercapto-, 2-propenyl ester, (2S-cis)-HCID 57280119—
SolventDichloromethaneHCID 6344—
ProductHCID 57030967HCID 5703096768%

Reaction Steps

To a solution of (2S,4S)-2-aminomethyl-1-allyloxycarbonyl-4-mercaptopyrrolidine (2.80 g: ca. 13.14 mmole) in dichloromethane (66 ml) at -50° C., triethylamine (4.02 ml: 28.91 mmole) and trimethylchlorosilane (3.76 ml: 28.91 mmole) are added dropwise over 15 minutes. The mixture is stirred at the same temperature for 20 minutes. To the reaction mixture triethylamine (0.92 ml: 6.57 mmole) and a solution of sulfamoyl chloride (19.37 mmole) in dichloromethane (6.8 ml) are added dropwise over 20 minutes at -70° C., and the mixture is stirred for 30 minutes. To the reaction mixture triethylamine (3.84 ml: 27.59 mmole) is again added over 1 hour at -50° C. The reaction mixture is kept at the same temperature overnight and concentrated in vacuo. The residual oil is purified by silica gel chromatography (ethyl acetate) to give (2S,4S)-1-allyloxycarbonyl-2-(sulfamoylamino)methyl-4-mercaptopyrrolidine (2.64 g). Yield: 68%. White powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703243
Source datasetuspto-grants-1997_12
ORD IDord-c99f35b21b7e4d59aefb947166b9e627
Source noteuspto-grants-1997_12