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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32517Generated: October 26, 2026

Methyl thieno[2,3-d]pyrimidine-6-carboxylate → N-Methoxy-N-methylthieno[2,3-d]pyrimidine-6-carboxamide

https://huagongshe.com/reaction/32517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl thieno[2,3-d]pyrimidine-6-carboxylateHCID 17965832—
ReactantMethoxy-methyl amideHCID 53630747—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductN-Methoxy-N-methylthieno[2,3-d]pyrimidine-6-carboxamideHCID 8592970767.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

iPrMgCl (2M in THF, 1.1 mL) was added dropwise to a solution of methyl thieno[2,3-d]pyrimidine-6-carboxylate (intermediate 11) (138 mg) and N-methoxy-N-methylamide (104 mg) in THF at −20° C. maintaining the internal temperature below −5° C. The reaction was allowed to stir at −10° C. for 30 minutes and then quenched with NH4Cl (sat. aq). The solution was diluted with EtOAc and the organic layer was separated. The aqueous layer was extracted with EtOAc (2×15 mL) and then the combined organics dried (MgSO4), filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with hexane:EtOAc (1:1 to 1:4) afforded the title compound as a pale yellow solid (107 mg, 67%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427616B2
Source datasetuspto-grants-2008_09
ORD IDord-8a8883e797c94e98bb80a4a28619efad
Source noteuspto-grants-2008_09