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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53242Generated: October 25, 2026

Diisopropylethylamine → N-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)methanesulfonamide

https://huagongshe.com/reaction/53242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(2-bromoethyl)methanesulfonamideHCID 285330—
Reactant4-PiperidinemethanolHCID 420771—
SolventAcetonitrileHCID 6342—
ProductN-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)methanesulfonamideHCID 1996211454.8%

Reaction Steps

4-Piperidine methanol (1.60 g) was dissolved in dry acetonitrile (40 ml), N,N-diisopropylethylamine (5 ml) was added, followed by N-(2-bromoethyl)methanesulphonamide (2.95 g) in acetonitrile (10 ml), and the resulting mixture heated at reflux for 2 h. The solvent was removed in vacuo to leave a gum. This was purified by FCC eluting with System A (75:8:1) to give the title compound (1.80 g) as a solid, m.p. 81°-82°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618827
Source datasetuspto-grants-1997_04
ORD IDord-b799967ecb2b40aeb1be5ec9736eebe1
Source noteuspto-grants-1997_04