HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911403Generated: October 26, 2026
Trimethylaluminum → HCID 178489802, compound
https://huagongshe.com/reaction/1911403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Methyl 2-(1,3,4,6,7,8,9,9a-octahydropyrido[2,1-c]pyrazin-2-yl)pyrimidine-5-carboxylate | HCID 66589987 | — |
| Reactant | HCID 178489815 | HCID 178489815 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178489802 | HCID 178489802 | 42% |
Reaction Steps
Trimethylaluminium (2M in toluene, 1.45 mL, 2.90 mmol) was added dropwise to a stirred suspension of 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (286 mg, 1.16 mmol) and methyl 2-(1,3,4,6,7,8,9,9a-octahydropyrido[2,1-c]pyrazin-2-yl)pyrimidine-5-carboxylate (320 mg, 1.16 mmol) in toluene (5.8 mL) at 25° C. The resulting solution was stirred at ambient temperature for 18 h and then at 60° C. for 2 h. The reaction mixture was quenched with methanol (20 mL) and treated with HCl (2N aqueous solution, until a freely stirred solution was obtained). The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and evaporated to dryness to afford impure product. The impure material was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 0.1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (238 mg, 42%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08604022B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-1ad90328a974401c94dca923af79897e |
|---|
| Source note | uspto-grants-2013_12 |
|---|