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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913070Generated: October 29, 2026

Acetic Acid → N-{3-[1-(3,5-Diethoxy-4-fluoro-benzyl)-piperidin-4-ylamino]-phenyl}-acetamide

https://huagongshe.com/reaction/913070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3,5-Diethoxy-4-fluoro-benzaldehydeHCID 59128273—
ReactantN-[3-(Piperidin-4-ylamino)-phenyl]-acetamide dihydrochlorideHCID 67400427—
SolventEthanolHCID 702—
ProductN-{3-[1-(3,5-Diethoxy-4-fluoro-benzyl)-piperidin-4-ylamino]-phenyl}-acetamideHCID 2485496923.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of N-[3-(piperidin-4-ylamino)-phenyl]-acetamide dihydrochloride (61.2 mg, 0.2 mmol, 1.0 equiv; intermediate B1), acetic acid (60.1 mg, 1.0 mmol, 5.0 equiv) and triethylamine (40.5 mg, 0.4 mmol, 2.0 equiv) in ethanol (1 mL) was added 3,5-diethoxy-4-fluoro-benzaldehyde (53.1 mg, 0.25 mmol, 1.25 equiv; intermediate E5, vide infra) and the mixture stirred at 50° C. After 1 h, sodium cyanoborohydride (15.1 mg, 0.24 mmol, 1.2 equiv), dissolved in ethanol (1 mL), was added and the mixture stirred at 50° C. over night. Removal of the solvent under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 19.9 mg (23%) of the title compound. MS (ISP): 430.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026255B2
Source datasetuspto-grants-2011_09
ORD IDord-5ed050fa6acf48f499242eb1248e31f1
Source noteuspto-grants-2011_09