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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406380Generated: October 26, 2026

1-Hydroxybenzotriazole → benzyl N'-[3-methoxy-4-(4-methylimidazol-1-yl)benzoyl]hydrazinecarboxylate

https://huagongshe.com/reaction/406380

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzyl carbazateHCID 79242—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoic acidHCID 57931763—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productbenzyl N'-[3-methoxy-4-(4-methylimidazol-1-yl)benzoyl]hydrazinecarboxylateHCID 66618835—

Reaction Steps

IPEA (1.05 mL) and 1-ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride (1.16 g) were sequentially added to a solution of 3-methoxy-4-(4-methylimidazol-1-yl)benzoic acid (CAS#937026-26-1, 933 mg), benzyl carbazate (737 mg) and HOBT (817 mg) in DMF (15 mL), and the mixture was stirred at room temperature overnight. Ethyl acetate, ice water and a saturated sodium bicarbonate solution were added to the reaction solution, and the organic layer was separated. The resulting organic layer was sequentially washed with water and brine. The combined aqueous layer was extracted with ethyl acetate. The combined organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. Ethyl acetate and NH silica gel were added to the resulting residue and then the mixture was concentrated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754100B2
Source datasetuspto-grants-2014_06
ORD IDord-b8bc32398b6b40d2b6d8d392cd925a9c
Source noteuspto-grants-2014_06