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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452586Generated: October 25, 2026

tert-Butyl carbazate → Tert-butyl 2-(benzothiazol-6-ylcarbonyl)hydrazinecarboxylate

https://huagongshe.com/reaction/452586

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbazateHCID 70091—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzothiazole-6-carboxylic acidHCID 601670—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(benzothiazol-6-ylcarbonyl)hydrazinecarboxylateHCID 6866365975.1%

Reaction Steps

A solution of benzothiazole-6-carboxylic acid (4.48 g, 25.0 mmol), tert-butyl carbazate (3.63 g, 27.5 mmol), 3-(3-dimethylaminopropyl)-1-ethylcarbodiimide hydrochloride (5.75 g, 30.0 mmol) and 1-hydroxybenzotriazole (4.05 g, 30.0 mmol) in N,N-dimethylformamide (50 mL) was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed twice with water and once with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate/tetrahydrofuran=2/1), and crystallized from hexane/acetone to give the title compound (5.51 g, yield 75%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-45370c378ca6432ca518cd20c6df846b
Source noteuspto-grants-2013_07