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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190309Generated: October 30, 2026

Trifluoroacetic acid → 3-(4-(Methylsulfonyl)phenyl)-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/2190309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantTert-butyl 3-(4-(methylsulfonyl)phenyl)-1,2,4-thiadiazol-5-ylcarbamateHCID 68743050—
SolventDichloromethaneHCID 6344—
Product3-(4-(Methylsulfonyl)phenyl)-1,2,4-thiadiazol-5-amineHCID 33780235—

Reaction Steps

To a solution of tert-butyl 3-(4-(methylsulfonyl)phenyl)-1,2,4-thiadiazol-5-ylcarbamate (1.57 g, 4.42 mmol) in DCM (20 mL) was added anisol (0.50 mL) and TFA (10 mL). The reaction mixture was stirred at room temperature for 6 h and concentrated. The solid was suspended in saturated NaHCO3 (˜200 mL) and stirred for 30 min. The solid was collected by filtration, washed with water (˜500 mL) followed by hexanes (˜50 mL), and dried under high vacuum to give 3-(4-(methylsulfonyl)phenyl)-1,2,4-thiadiazol-5-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324396B2
Source datasetuspto-grants-2012_12
ORD IDord-b3d19bf62c444c7f9aad97744038cd74
Source noteuspto-grants-2012_12