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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930509Generated: October 29, 2026

3-Methyl-2-furoic acid → US9296747, Example 11

https://huagongshe.com/reaction/930509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-2-furoic acidHCID 78127—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantN-(3,4,5-Trimethoxyphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amineHCID 118970894—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductUS9296747, Example 11HCID 11897089947.3%

Reaction Steps

A solution of (Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium-hexafluorophosphate (0.035 g, 0.079 mmol) in anhydrous DMF (2 mL) was treated sequentially with 3-methylfuran-2-carboxylic acid (0.013 g, 0.103 mmol) and diisopropylethylamine (0.035 mL, 0.159 mmol). The reaction mixture was allowed to stir for 30 minutes at room temperature. After 30 minutes, N-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amine, Intermediate 1 (0.025 g, 0.079 mmol) was added to the reaction mixture. The reaction was allowed to stir for 3 hours at room temperature. The reaction mixture was then diluted with EtOAc and washed three times with brine. The combined aqueous layers were then washed twice with EtOAc. The organic layers were combined, dried over anhydrous Na2SO4(s), filtered and concentrated in vacuo. The crude product was then purified over silica using a MeOH/CHCl3 gradient affording the final product in 47.3% yield (0.014 g, 0.037 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296747B1
Source datasetuspto-grants-2016_03
ORD IDord-b367f269be634e92a4a5a9e305a3c1bc
Source noteuspto-grants-2016_03