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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978955Generated: October 26, 2026

Methanol → HCID 178496975, compound

https://huagongshe.com/reaction/1978955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 178522942HCID 178522942—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 178496975HCID 178496975—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of N-(4-chlorobenzyl)-4-hydroxy-2-iodothieno[2,3-b]pyridine-5-carboxamide (2.61 g) from Example No. 2 in DMF (33 mL) are added triethylamine (1.6 mL), methanol (9.5 mL), Pd(OAc)2 (0.132 g), and dppp (0.242 g). Carbon monoxide is bubbled through the solution, and the reaction is heated to 70° C. The reaction is stirred at 70° C. for 18 h. The reaction mixture is cooled to rt, and water (25 mL) and 2 N HCl (25 mL) are added. The resulting precipitate is filtered off and purified by column chromatography (CH2Cl2; CH2Cl2/methanol, 99/1; 98/2). A mixture of starting material and desired product is isolated as a yellow solid. This material is re-subjected to the reaction conditions above. The reaction is stirred at 70° C. for 18 h. The reaction is cooled to rt and water (25 mL) and 2 N HCl (25 mL) are added. The resulting orange solid is filtered off and purified by column chromatography (CH2Cl2;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239142B1
Source datasetuspto-grants-2001_05
ORD IDord-7f2ccaadcc2647e8a2f7c5854b9ccfea
Source noteuspto-grants-2001_05