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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341989Generated: October 30, 2026

Nitrogen → HCID 54537147, compound

https://huagongshe.com/reaction/341989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTriethylamineHCID 8471—
ReactantCesium carbonateHCID 10796—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethanesulfonateHCID 85257—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 3-mercapto-2-methylpropanoateHCID 15289599—
ReactantHCID 53725555HCID 53725555—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 54537147HCID 54537147—

Reaction Conditions

Temperature-10 °C

Reaction Steps

At -40° C., Et3N (triethylamine) (1.60 mL, 11.5 mmol) and methanesulfonyl chloride (750 μl, 9.69 mmol) were added to a solution of the alcohol of Step 6 (7.39 mmol) in 74 mL of CH2Cl2 and the mixture was stirred at -40° C. for an hour and at -10° C. for 45 minutes. Saturated aq NaHCO3 was then added and the mesylate was extracted with CH2Cl2, dried over Na2SO4 and concentrated. To this mesylate in 150 mL of anhydrous CH3CN, ethyl 3-mercapto-2-methylpropanoate (Example 4, Step 6; 2.20 mL, approx. 15 mmol) and Cs2CO3 (7.57 g, 23.2 mmol) were added and the mixture was stirred under a stream of N2 for 2 hours. 25% Aq NH4OAc was then added and the title product was extracted with EtOAc, dried over Na2SO4 and purified by flash chromatography on silica with EtOAc:toluene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856322
Source datasetuspto-grants-1999_01
ORD IDord-328432b498644acdb9f83d105769bbc6
Source noteuspto-grants-1999_01