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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056965Generated: October 26, 2026

tert-Butyl 4-(2-bromoethyl)piperidine-1-carboxylate → tert-Butyl 4-{2-[6-bromo-7-(cyclobutylmethoxy)-3-methyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]ethyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1056965

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2-bromoethyl)piperidine-1-carboxylateHCID 10541625—
Reactant5-bromo-4-(cyclobutylmethoxy)-1-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 118093901—
Producttert-Butyl 4-{2-[6-bromo-7-(cyclobutylmethoxy)-3-methyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]ethyl}piperidine-1-carboxylateHCID 118093808—

Reaction Steps

This compound was synthesized according to the procedure of Example 44, Step 2, using 5-bromo-4-(cyclobutylmethoxy)-1-methyl-1,3-dihydro-2H-benzimidazol-2-one and tert-butyl 4-(2-bromoethyl)piperidine-1-carboxylate as the starting materials. LCMS calculated for C20H29BrN3O2 ([M-Boc+H]+H)+: m/z=422.2, 424.2. found: 422.0, 424.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399640B2
Source datasetuspto-grants-2016_07
ORD IDord-e6c4dd697b064751a5cf229d557d05c7
Source noteuspto-grants-2016_07