HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092122Generated: November 2, 2026
Trimethylaluminum → HCID 178489811, compound
https://huagongshe.com/reaction/1092122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 66589787 | HCID 66589787 | — |
| Reactant | HCID 178489815 | HCID 178489815 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178489811 | HCID 178489811 | 62.1% |
Reaction Steps
Trimethylaluminium (2M in toluene, 1.23 mL, 2.46 mmol) was added dropwise to a stirred suspension of (S)-methyl 2-(3-prop an-2-ylpiperazin-1-yl)pyrimidine-5-carboxylate (260 mg, 0.98 mmol) and 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (243 mg, 0.98 mmol) in toluene (8.38 mL) at room temperature. The reaction was then stirred at 60° C. for 18 h under a nitrogen atmosphere. The reaction mixture was quenched into methanol (100 mL) and treated with HCl (2N aqueous solution, until the pH was 7 or lower). The crude product was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness to afford impure product. The crude product was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (292 mg, 62%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129391B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-488bdbf657f249d6a2a5803e2011442d |
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| Source note | uspto-grants-2012_03 |
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