Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006201Generated: October 25, 2026

Pyridine → ({[4-(3-Bromo-4-methoxy-phenoxy)-3,5-dimethyl-phenyl]-hydrazono}-cyano-acetyl)-carbamic acid ethyl ester

https://huagongshe.com/reaction/1006201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthylcyanoacetylurethaneHCID 12693910—
Reactant4-(3-Bromo-4-methoxy-phenoxy)-3,5-dimethyl-phenylamineHCID 22339502—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product({[4-(3-Bromo-4-methoxy-phenoxy)-3,5-dimethyl-phenyl]-hydrazono}-cyano-acetyl)-carbamic acid ethyl esterHCID 86593878—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 4-(3-bromo-4-methoxy-phenoxy)-3,5-dimethyl-phenylamine (2.0 g) of PREPARATION 2 in 6N hydrochloric acid (45 ml) at 0° C. was added dropwise a solution of sodium nitrite (560 mg) in water (1.25 ml). After stirring 30 min at 0° C., this solution was added in portions to a mixture of ethylcyanoacetylurethane (2.4 g) and pyridine (12 ml) in water (150 ml) at room temperature. The resulting solids were collected, washed with water, and dried to afford the title compound as an orange solid (1.5 g) which was used directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787652B1
Source datasetuspto-grants-2004_09
ORD IDord-010eaf3ee93346b0a1c0f1f0cf7077bb
Source noteuspto-grants-2004_09