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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368276Generated: November 1, 2026

Methylamine → Carbamic acid, N-[4-[(methylamino)carbonyl]-1,2,3-thiadiazol-5-yl]-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/2368276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 70116272HCID 70116272—
SolventDimethylformamideHCID 6228—
ProductCarbamic acid, N-[4-[(methylamino)carbonyl]-1,2,3-thiadiazol-5-yl]-, 1,1-dimethylethyl esterHCID 70115888—

Reaction Steps

A solution of 5-tert-butoxycarbonylamino-[1,2,3]thiadiazole-4-carboxylic acid (0.66 g, 2.7 mmol) in DMF (10 ml) was treated with TBTU (1.16 g, 3.5 mmol), N,N-diisopropyl ethyl amine (2.29 ml, 13.5 mmol) and methylamine (1.75 ml, 2M THF solution) and stirred at ambient temperature for 5 h. The reaction mixture was partitioned between potassium hydrogen sulfate (30 ml, 10% aqueous solution) and ethyl acetate (60 ml) and extracted. The organic layer was washed with water and brine, and the aqueous phases were back-extracted with ethyl acetate. The combined organic phases were dried and the solvent was evaporated. The residue was suspended in dichloromethane, sucked off, and the filtrate was evaporated. The product was obtained after purification of the crude material by silica gel chromatography using a heptane/ethyl acetate gradient as colorless solid (0.23 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703768B2
Source datasetuspto-grants-2014_04
ORD IDord-62a07876ee464471ab9850a50131028b
Source noteuspto-grants-2014_04