Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067319Generated: November 1, 2026

Pyridine → Ethyl 2-(hydrazinecarboxamido)-4-methylthiazole-5-carboxylate

https://huagongshe.com/reaction/2067319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantEthyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(hydrazinecarboxamido)-4-methylthiazole-5-carboxylateHCID 8663520278%

Reaction Steps

To a solution of ethyl 2-amino-4-methylthiazole-5-carboxylate (0.50 g, 2.68 mmol) and pyridine (0.32 mL, 4.03 mmol) in tetrahydrofuran (25 mL) and dichloromethane (25 mL) was added 4-nitrophenyl chloroformate (0.65 g, 3.22 mmol) at 0° C. The resulting reaction mixture was stirred at ambient temperature for 1 hour, followed by the addition of hydrazine monohydrate (3.00 mL, 59.9 mmol). The reaction mixture was stirred at ambient temperature for 18 hours and quenched with water (100 mL). The solid precipitated was filtered, washed with water and ethyl acetate and dried to afford the title compound in 78% yield (0.51 g): MS (ES+) m/z 245.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293768B2
Source datasetuspto-grants-2012_10
ORD IDord-c4163074333c47279907b4aa3e2d3d9a
Source noteuspto-grants-2012_10