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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42157Generated: October 25, 2026

Tert-butyl 4-[2-(4-methanesulfonyl-phenoxymethyl)pyridin-5-yl]piperidine-1-carboxylate → 2-[4-[2-(4-Methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]-5-pentylpyrimidine

https://huagongshe.com/reaction/42157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-[2-(4-methanesulfonyl-phenoxymethyl)pyridin-5-yl]piperidine-1-carboxylateHCID 44819975—
ReactantHCID 86654266HCID 86654266—
Product2-[4-[2-(4-Methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]-5-pentylpyrimidineHCID 67083133—

Reaction Steps

The title compound was prepared from tert-butyl 4-[2-(4-methanesulfonylphenoxymethyl)pyridin-5-yl]piperidine-1-carboxylate (Example 1) (50 mg, 0.11 mmol) and 5-pentyl-2-bromopyrimidine (37 μL, 0.22 mmol) following a procedure analogous to that in Example 48 as a white crystal (35 mg, yield 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536176B2
Source datasetuspto-grants-2013_09
ORD IDord-e8436764dc3747dababb18eb91fd24a0
Source noteuspto-grants-2013_09