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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792286Generated: November 3, 2026

HCID 22034100, compound → HCID 22034139, compound

https://huagongshe.com/reaction/1792286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22034100HCID 22034100—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22034139HCID 22034139—

Reaction Steps

Add BH3 in THF (1 M solution, 0.3 mmol, 0.3 mL) to a solution of the crude 2-(3,4-dimethoxyphenyl)-N-(2-{[3,6-dimethyl-2-(2,4,6-trimethylphenoxy)(4-pyridyl)]amino}ethyl) acetamide in THF (2.0 mL) at ambient temperature. Heat the reaction mixture under reflux for 15 h, dilute with a solution of 10% aq HCV/MeOH (1:1, 2 mL) and heat again under reflux (1 h). Dilute the reaction mixture with CHCl3 (10 mL), wash with saturated aq NaHCO3 (1×5 mL), dry and concentrate in vacuo. Chromatograph the crude residue on SiO2-gel using a gradient of 100% EtOAc to 10% Et2NH/EtOAc to obtain the title compound as a colorless oil. Immediately dissolve the product in Et2O (1 mL), treat with excess 4 M HCl/dioxane and concentrate in vacuo to obtain the hydrochloride salt of the title compound as a colorless solid. 1H NMR (d4-MeOH, Unity 400): d 6.99–6.77 (6H, m), 3.81 (3H, s), 3.78 (3H, s), 3.62 (2H, m), 2.98 (2H, t), 2.39 (3H, s), 2.29 (3H, s), 2.16 (3H, s), 2.07 (6H, s). M+1: 464.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074929B2
Source datasetuspto-grants-2006_07
ORD IDord-6f046879ca3246f4b57f746bea94b86f
Source noteuspto-grants-2006_07