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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352440Generated: October 30, 2026

Triethylamine → HCID 10145374, compound

https://huagongshe.com/reaction/352440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 11469921HCID 11469921—
ReactantHCID 11488562HCID 11488562—
SolventAcetoneHCID 180—
ProductHCID 10145374HCID 1014537446.2%

Reaction Steps

4.7 g of 4-[cyclopropylmethyl-(3-hydroxy-propyl)-amino]-piperidine are stirred together with 9.6 g of (R)—N-[2-(3,5-bis-trifluoromethyl-phenyl)-ethyl]-2-methanesulphonyloxy-N-methyl-2-phenyl-acetamide (prepared from D-(−)-mandelic acid) and 3.4 ml of triethylamine in 200 ml of acetone for four hours at 65° C. The mixture is concentrated by evaporation in vacuo, combined with 100 ml of saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The combined organic fractions are dried over sodium sulphate and the solvent is eliminated in vacuo. The residue is chromatographed with methylene chloride/methanol 1:1 over silica gel. The fractions found to be uniform by TLC are collected and the solvents are eliminated in vacuo. 5.5 g of (S)—N-[2-(3,5-bis-trifluoromethyl-phenyl)-ethyl]-2-{4-[cyclopropylmethyl-(3-hydroxy-propyl)-amino]-piperidin-1-yl}-N-methyl-2-phenyl-acetamide are obtained as a brownish-yellow oil, [α]D20=+35.1°

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747044B2
Source datasetuspto-grants-2004_06
ORD IDord-96eb1e066c3349f486da4033b8d3ef49
Source noteuspto-grants-2004_06