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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183481Generated: November 4, 2026

Triethylamine → 3-Cyano-5-hydroxymethyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-6-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/2183481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(4-Aminophenoxy)benzeneHCID 8764—
Reactant4-Chloro-3-cyano-5-hydroxymethyl-pyrrolo[1,2-b]pyridazine-6-carboxylic Acid Ethyl EsterHCID 20791627—
SolventTetrahydrofuranHCID 8028—
Product3-Cyano-5-hydroxymethyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-6-carboxylic Acid Ethyl EsterHCID 2079160192%

Reaction Steps

A solution of compound 16B (84 mg, 0.30 mmol), 4-phenoxyaniline (72 mg, 0.39 mmol) and triethylamine (0.083 mL, 0.60 mmol) in THF (2.5 mL) was heated at 70° C. for 30 min. After cooled to room temperature, the reaction was concentrated to about 0.5 mL, diluted with MeOH (2 mL) and filtered. The solid was washed with MeOH and dried to give compound 16C as a yellow solid (118 mg, 92%). HPLC: 92% at 2.12 min (retention time) (PrimeSphere 5u C18-HC column, 4.6×30 mm eluting with 10-90% MeOH/H2O over 2 minutes containing 0.1% TFA; mL/min, monitoring at 220 nm). MS (ES): m/z 429.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900208B2
Source datasetuspto-grants-2005_05
ORD IDord-e1114a132dac44af8ecc84fe7775c1c3
Source noteuspto-grants-2005_05