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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458611Generated: October 26, 2026

Sodium Carbonate → N-[(1-n butyl-4-piperidyl)methyl] 2-(4-chlorobutoxy)indole-3-carboxamide

https://huagongshe.com/reaction/1458611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chloro-1-butanolHCID 13569—
ReactantChlorosuccinimideHCID 31398—
ReactantN-[(1-n butyl-4-piperidyl)methyl] indole-3-carboxamideHCID 10591304—
SolventChloroformHCID 6212—
ProductN-[(1-n butyl-4-piperidyl)methyl] 2-(4-chlorobutoxy)indole-3-carboxamideHCID 1050219750%

Reaction Steps

A stirred suspension of N-[(l-n butyl-4-piperidyl)methyl] indole-3-carboxamide (Description 1b, 1.0 g, 0.0032 mole) in chloroform (25 ml) was treated with 4-chlorobutanol (0.69 ml, 0.0064 mole) followed by N-chlorosuccinimide (470 mg, 0.0035 mole) and a yellow solution was produced inside 5 minutes. After a further 40 minutes the solution was observed to darken in colour to orange. The mixture was kept at room temperature for a further 1 h then treated with 10% Na2CO3 solution (30 ml) and extracted with chloroform (2×30 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to afford an orange oil, which was chromatographed on silica gel eluting with 5% methanol/chloroform to give N-[(1-n butyl-4-piperidyl)methyl] 2-(4-chlorobutoxy)indole-3-carboxamide (0.67 g, 50%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852014
Source datasetuspto-grants-1998_12
ORD IDord-c0b0591d219a41db87803f103668d32d
Source noteuspto-grants-1998_12