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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911360Generated: November 1, 2026

Ammonium Chloride → n-[5-[2-(3,5-Dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(1-methyl-4-piperidyl)benzamide

https://huagongshe.com/reaction/1911360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantMethyl 4-(1-methylpiperidin-4-YL)benzoateHCID 49760144—
ReactantTert-butyl 5-amino-3-[2-(3,5-dimethoxyphenyl)ethyl]pyrazole-1-carboxylateHCID 57440371—
SolventTetrahydrofuranHCID 8028—
Productn-[5-[2-(3,5-Dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(1-methyl-4-piperidyl)benzamideHCID 6659006216.1%

Reaction Steps

A solution of NaHMDS (1M in THF) (5.91 mL, 5.91 mmol) was added dropwise to a stirred solution of methyl 4-(1-methylpiperidin-4-yl)benzoate (0.4594 g, 1.97 mmol) and tert-butyl 5-amino-3-[2-(3,5-dimethoxyphenyl)ethyl]-1H-pyrazole-1-carboxylate (0.821 g, 2.36 mmol) in THF (4 mL), over a period of 10 mins under nitrogen. The resulting solution was stirred at room temperature for 18 h. The reaction mixture was poured into saturated NH4Cl (25 mL), extracted with EtOAc (2×25 mL), washed with saturated brine and dried over MgSO4, filtered and evaporated to afford the crude product (1.0719 g) as an orange gum. 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 (0.142 g, 16.08%) as a white solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-6eea2be97fbc454eb5b4b6ae1879192a
Source noteuspto-grants-2013_12