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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131400Generated: October 31, 2026

Pyridine → (S)-4-benzyl-2-(2-methanesulfonyloxy-ethyl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/131400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-4-Benzyl-2-(2-hydroxyethyl)piperazine-1-carboxylic acid tert-butyl esterHCID 15406045—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductAmmonia methanolHCID 217058975%
Product(S)-4-benzyl-2-(2-methanesulfonyloxy-ethyl)piperazine-1-carboxylic acid tert-butyl esterHCID 86604576123.5%

Reaction Steps

To a solution of (S)-4-benzyl-2-(2-hydroxyethyl)piperazine-1-carboxylic acid tert-butyl ester (4.87 g, 15.2 mmol) in dichloromethane (200 mL), add pyridine (1.84 mL, 22.8 mmol) followed by methanesulfonyl chloride (1.29 mL, 16.7 mmol). Stir at room temperature overnight, then dilute with saturated aqueous sodium bicarbonate. Extract three times with dichloromethane; dry combined organic extracts over sodium sulfate, filter and concentrate in vacuo to give a brown residue. Redissolve residue in dichloromethane and apply to a plug of silica gel. Wash plug with 5% 2N ammonia-methanol in dichloromethane to obtain (S)-4-benzyl-2-(2-methanesulfonyloxy-ethyl)piperazine-1-carboxylic acid tert-butyl ester (3.74 g, 62%) as a yellow-brown thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-7515a520812d4d84adc1e86c622dea02
Source noteuspto-grants-2008_06