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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485367Generated: October 30, 2026

Water → Phenyl (3-methoxy-1,2,4-thiadiazol-5-yl)carbamate

https://huagongshe.com/reaction/1485367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant5-Amino-3-methoxy-1,2,4-thiadiazoleHCID 314179—
SolventDichloromethaneHCID 6344—
ProductPhenyl (3-methoxy-1,2,4-thiadiazol-5-yl)carbamateHCID 89664142—

Reaction Steps

3-Methoxy-1,2,4-thiadiazol-5-amine a (500 mg, 3.82 mmol) and phenyl carbonochloridate b (600 mg, 3.82 mmol) were dissolved in 20 mL of dichloromethane, followed by addition of triethylamine (0.8 mL, 5.73 mmol). After reacting for 16 hours, 30 mL of H2O were added into the reaction mixture to dilute the solution. The aqueous phase and organic phase were separated, the aqueous phase was extracted with dichloromethane (20 mL×2), and the organic phases were combined, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography with elution system A to obtain the title product phenyl(3-methoxy-1,2,4-thiadiazol-5-yl)carbamate c (200 mg, yield 20.8%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422300B2
Source datasetuspto-grants-2016_08
ORD IDord-b4051da75b034c87b5f5f3736894c63d
Source noteuspto-grants-2016_08