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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183482Generated: November 2, 2026

Methanol → 4-Chloro-3-cyano-5-methoxymethyl-pyrrolo[1,2-b]pyridazine-6-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/2183482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromomethyl-4-chloro-3-cyano-pyrrolo[1,2-b]pyridazine-6-carboxylic Acid Ethyl EsterHCID 20791631—
SolventDichloromethaneHCID 6344—
Product4-Chloro-3-cyano-5-methoxymethyl-pyrrolo[1,2-b]pyridazine-6-carboxylic Acid Ethyl EsterHCID 2079162898.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of compound 16A (31 mg, 0.09 mmol) in 1:1 MeOH:CH2Cl2 (2 mL) was added NaHCO3 (30 mg, 0.36 mmol). The reaction was kept at room temperature for 3 h, heated to 70° C. for 1 h, cooled to room temperature, concentrated to dryness, redissolved in CH2Cl2 and filtered. The filtrate was concentrated to give compound 17A as a yellow solid (26 mg, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900208B2
Source datasetuspto-grants-2005_05
ORD IDord-879141e1d5bb483f970ee6f13b75835a
Source noteuspto-grants-2005_05