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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170514Generated: October 31, 2026

Potassium Carbonate → Benzyl 2-(3-amino-1,2,4-thiadiazol-5-YL)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1170514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Acetylamino-[1,2,4]thiadiazol-5-yl)-pyrrolidine-1-carboxylic acid benzyl ester hydrobromideHCID 68695659—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductBenzyl 2-(3-amino-1,2,4-thiadiazol-5-YL)pyrrolidine-1-carboxylateHCID 5343603094%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(3-Acetylamino-[1,2,4]thiadiazol-5-yl)-pyrrolidine-1-carboxylic acid benzyl ester hydrobromide (14.0 g, 37.8 mmol) was dissolved in ethanol (80 mL). The reaction mixture was cooled to 0° C. and a solution of K2CO3 (15.0 g, 108.7 mmol) in H2O (40 mL) was added. The solution was allowed to return to room temperature while stirring for 30 mins. The solution was concentrated down, redissolved in water (100 mL) and extracted with DCM (3×50 mL). The organic layers were combined and washed with brine (3×50 mL). The organic layer was partitioned from the aqueous layer, dried over MgSO4 and concentrated under vacuo to afford 9.4 g (94%) of 2-(3-amino-[1,2,4]thiadiazol-5-yl)-pyrrolidine-1-carboxylic acid benzyl ester as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825256B2
Source datasetuspto-grants-2010_11
ORD IDord-52e89bc613294643ba254eabd0ffe2bc
Source noteuspto-grants-2010_11