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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911480Generated: October 27, 2026

Trimethylaluminum → HCID 178489784, compound

https://huagongshe.com/reaction/1911480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylaluminumHCID 16682925—
ReactantMethyl 2-(4-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylateHCID 66589974—
ReactantHCID 178489815HCID 178489815—
SolventTolueneHCID 1140—
ProductHCID 178489784HCID 1784897841.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

Trimethylaluminium (1.402 ml, 2.80 mmol) was added dropwise to a stirred suspension of methyl 2-(4-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate (310 mg, 1.12 mmol) and 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (277 mg, 1.12 mmol) in toluene (5.61 ml) at 25° C. The resulting solution was stirred at 60° C. for 18 h. The cooled reaction mixture was quenched into methanol (50 mL) and treated with HCl (2M aqueous solution, to pH7 or lower) and purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and 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 (8.00 mg, 1%) as a cream solid. Some impure fractions were combined and concentrated to dryness and purified by crystallisation from MeCN to afford the title compound (51 mg, 9%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-55d897091436495d8fb8bf83144ce9f3
Source noteuspto-grants-2013_12