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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202201Generated: October 29, 2026

Water → HCID 86675029, compound

https://huagongshe.com/reaction/2202201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-Propanesulfonyl chloride, 2-methyl-HCID 182236—
ReactantHCID 86675027HCID 86675027—
SolventDichloromethaneHCID 6344—
ProductHCID 86675029HCID 8667502971%

Reaction Conditions

Temperature0 °C

Reaction Steps

479 mg (3.0 mmol) of 2-methylpropane-1-sulfonyl chloride are added to a solution of 800 mg (2.8 mmol) of methyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoate (prepared as described in example 23.1) and 775 μl (5.5 mmol) of triethylamine in 8 ml of dichloromethane, cooled beforehand to 0° C. The reaction medium is stirred at ambient temperature for 18 h and then water is added and the medium is extracted with dichloromethane. The organic phase is washed with water, dried over magnesium sulfate, filtered and concentrated. The residue obtained is purified by chromatography on silica gel, elution being carried out with a 5/5 heptane/ethyl acetate mixture. 785 mg (71%) of methyl (S)-3-tert-butoxycarbonylamino-2-[4-(2-methylpropane-1-sulfonyl)piperazin-1-yl]propanoate are obtained in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-751c9b6139374107881a6c97cbd59a83
Source noteuspto-grants-2016_06