Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175413Generated: October 29, 2026

Lawesson's reagent → 5-(Tert-butoxycarbonylamino-methyl)-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2175413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantEthyl (N-{2-[(tert-butoxy)carbonylamino]acetylamino}carbamoyl)formateHCID 10108216—
SolventTetrahydrofuranHCID 8028—
Product5-(Tert-butoxycarbonylamino-methyl)-[1,3,4]thiadiazole-2-carboxylic acid ethyl esterHCID 86729572261.8%

Reaction Steps

To the solution of ethyl 2-(2-(2-(tert-butoxycarbonylamino)acetyl) hydrazinyl)-2-oxoacetate (9-4) (228 mg, 0.6913 mmol) in THF (10 mL) was added lawesson's reagent (354 mg, 0.8669 mmol). The solution was heated to reflux for 3 h. Then solvent was evaporated under reduced pressure and the residue was purified by chromatography on silica gel with the eluant (PE/EA/NEt3=10/1/1%; 5/1/1%; 2/1/1%). The yellow solid was obtained as the product (520 mg, 69%). 1H NMR (500 MHz, CDCl3) δ 5.31 (br, 1H), 4.76 (d, J=6.1 Hz, 2H), 4.51 (d, J=14, 7.1 Hz, 2H), 1.60-1.39 (m, 12H); LRMS (ESI) calculated M+H for C11H18N3O4S: 288.3; Found: 288.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062059B2
Source datasetuspto-grants-2015_06
ORD IDord-322551a325304b1dab48274c9133c7ef
Source noteuspto-grants-2015_06