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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176434Generated: October 31, 2026

HCID 66668749, compound → HCID 66664953, compound

https://huagongshe.com/reaction/2176434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66668749HCID 66668749—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 66664953HCID 66664953—

Reaction Steps

tert-butyl 4-(2-(3-nitrophenyl)-5-oxo-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-7-yl)piperazine-1-carboxylate (220, 0.480 mmol, 1.0 equiv) is dissolved in 5 mL methanol. To the solution is added palladium on carbon (51.1 mg). The reaction is stirred under an atmosphere of hydrogen for 3 h. Upon completion, the mixture is filtered through celite and concentrated in vacuo to give crude tert-butyl 4-(2-(3-aminophenyl)-5-oxo-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-7-yl)piperazine-1-carboxylate as a yellow solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.37 (s, 1H), 7.20-7.29 (m, 1H), 7.13 (d, J=7.83 Hz, 1H), 6.83 (dd, J=7.63, 1.76 Hz, 1H), 5.46 (s, 1H), 3.87 (s, 2H), 3.45-3.65 (m, 8H), 1.48 (m, 9H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066948B2
Source datasetuspto-grants-2015_06
ORD IDord-141acc5508dd42d1a74fcf1cb23e142c
Source noteuspto-grants-2015_06