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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035702Generated: October 30, 2026

Trifluoroacetic acid → 4-amino-N-(5-benzyl[1.3.4]thiadiazol-2-yl)-benzamide

https://huagongshe.com/reaction/1035702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl [4-(5-benzyl[1.3.4]thiadiazol-2-ylcarbamoyl)phenyl]carbamateHCID 86662112—
SolventDichloromethaneHCID 6344—
Product4-amino-N-(5-benzyl[1.3.4]thiadiazol-2-yl)-benzamideHCID 6673994892.1%

Reaction Steps

0.2 g of tert-butyl [4-(5-benzyl[1.3.4]thiadiazol-2-ylcarbamoyl)phenyl]carbamate (0.49 mmol, 1 eq.) is placed in 5 mL of dichloromethane. 1 mL of trifluoroacetic acid (13.54 mmol, 27.6 eq.) is added and the reaction medium is stirred for 3 days at room temperature. The solvents are evaporated off and the residue is taken up in diethyl ether and pentane to give 0.14 g of 4-amino-N-(5-benzyl[1.3.4]thiadiazol-2-yl)-benzamide acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546391B2
Source datasetuspto-grants-2013_10
ORD IDord-d4284ddb46264b769d984419f915c718
Source noteuspto-grants-2013_10