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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858697Generated: October 26, 2026

1H-Benzimidazole, 2-(chloromethyl)-1-ethyl- → tert-butyl (3RS,4RS,5SR)-4-(4-chloro-phenyl)-3-(1-ethyl-1H-benzimidazol-2-ylmethoxy)-5-propyl-piperidine-1-carboxylate

https://huagongshe.com/reaction/1858697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Benzimidazole, 2-(chloromethyl)-1-ethyl-HCID 12408432—
Reactanttert-butyl (3RS,4RS,5SR)-4-(4-chloro-phenyl)-3-hydroxy-5-propyl-piperidine-1-carboxylateHCID 86604427—
Producttert-butyl (3RS,4RS,5SR)-4-(4-chloro-phenyl)-3-(1-ethyl-1H-benzimidazol-2-ylmethoxy)-5-propyl-piperidine-1-carboxylateHCID 86604429—

Reaction Steps

In an analogous manner to that described in Example 62(h), by alkylating tert-butyl (3RS,4RS,5SR)-4-(4-chloro-phenyl)-3-hydroxy-5-propyl-piperidine-1-carboxylate with 2-chloromethyl-1-ethyl-1H-benzoimidazole [Acta Pol. Pharm. 1977, 34(4), 359-369] there was obtained tert-butyl (3RS,4RS,5SR)-4-(4-chloro-phenyl)-3-(1-ethyl-1H-benzimidazol-2-ylmethoxy)-5-propyl-piperidine-1-carboxylate as a colourless oil, MS: 495 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-4b2500f0a1be40f0a4fc5a7e7d3f03be
Source noteuspto-grants-2000_11