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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930510Generated: November 1, 2026

Diisopropylethylamine → US9296747, Example 12

https://huagongshe.com/reaction/930510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant1,3-Dimethyl-1H-pyrazole-5-carboxylic acidHCID 587721—
ReactantN-(3,4,5-Trimethoxyphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amineHCID 118970894—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductUS9296747, Example 12HCID 11897089352%

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 1,3-dimethyl-1H-pyrazole-5-carboxylic acid (0.014 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 52% yield (0.018 g, 0.041 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296747B1
Source datasetuspto-grants-2016_03
ORD IDord-35989c4d72e0421fa19cd657c8a9e429
Source noteuspto-grants-2016_03