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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl thieno[2,3-d]pyrimidine-6-carboxylate | HCID 17965832 | — |
| Reactant | Methoxy-methyl amide | HCID 53630747 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Methoxy-N-methylthieno[2,3-d]pyrimidine-6-carboxamide | HCID 85929707 | 67.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07427616B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-8a8883e797c94e98bb80a4a28619efad |
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| Source note | uspto-grants-2008_09 |
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