Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371548Generated: November 1, 2026

Sodium Bicarbonate → N-(4-(5-amino-1,3,4-thiadiazol-2-yl)-1,2,5-oxadiazol-3-yl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/1371548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantThiosemicarbazideHCID 2723789—
ReactantN-(4-cyano-1,2,5-oxadiazol-3-yl)-2,2,2-trifluoroacetamideHCID 21071304—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(4-(5-amino-1,3,4-thiadiazol-2-yl)-1,2,5-oxadiazol-3-yl)-2,2,2-trifluoroacetamideHCID 2107130351%

Reaction Steps

To a suspension of N-(4-cyano-1,2,5-oxadiazol-3-yl)-2,2,2-trifluoroacetamide (0.10 g, 0.49 mmol) in 2 mL of TFA was added thiosemicarbazide (0.044 g, 0.49 mmol). The reaction mixture was poured into ice and neutralized with sat. NaHCO3 to pH=7. The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layer was washed with NaCl and concentrated. Trituration with diethyl ether afforded the title compound as a beige solid (0.070 g, 51%). 1H NMR (DMSO, 500 MHz) δ 7.93 (s, 2H), 6.55 (s, 1H). Mass Spec. FIA MS 281.1(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157476B2
Source datasetuspto-grants-2007_01
ORD IDord-d413def3779048aeb57fbb9a90a9c402
Source noteuspto-grants-2007_01