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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868868Generated: October 27, 2026

tert-Butyl 3-(2-bromoethyl)piperidine-1-carboxylate → tert-butyl 3-[2-(5-fluoro-3-iodo-1H-indazol-1-yl)ethyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/868868

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-(2-bromoethyl)piperidine-1-carboxylateHCID 21188829—
ReactantHCID 178505475HCID 178505475—
Producttert-butyl 3-[2-(5-fluoro-3-iodo-1H-indazol-1-yl)ethyl]piperidine-1-carboxylateHCID 8672315756%

Reaction Steps

The title compound was prepared in 56% yield from 5-fluoro-3-iodo-indazole and tert-butyl 3-(2-bromoethyl)piperidine-1-carboxylate according to the general procedure for Preparation 10A. 1H NMR (400 MHz, CDCl3): δ 1.16-1.32 (2H, m), 1.37-1.62 (11H, m), 1.78-1.87 (3H, m), 2.70-2.76 (1H, m), 2.90-2.93 (1H, m), 3.75-3.88 (2H, m), 4.42 (2H, t, J=2.0, 7.2 Hz), 7.11 (1H, d, J=8.4 Hz), 7.21 (1H, td, J=2.0, 8.8 Hz), 7.38 (1H, dd, J=4.0, 9.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969343B2
Source datasetuspto-grants-2015_03
ORD IDord-a9c60bbe70f54e9e942ee327c939e1cd
Source noteuspto-grants-2015_03