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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42171Generated: October 29, 2026

2-Methyl-4-(methylsulfonyl)phenol → Tert-Butyl 4-[2-(4-methanesulfonyl-2-methylphenoxymethyl)-3-methylpyridin-5-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/42171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-(methylsulfonyl)phenolHCID 12619667—
ReactantTert-Butyl 4-[2-(2-chloro-4-methanesulfonylphenoxymethyl)-3-methylpyridin-5-yl]piperidine-1-carboxylateHCID 86654270—
ProductTert-Butyl 4-[2-(4-methanesulfonyl-2-methylphenoxymethyl)-3-methylpyridin-5-yl]piperidine-1-carboxylateHCID 8665426930%

Reaction Steps

The title compound was prepared from tert-butyl 4-[(2-hydroxymethyl)-3-methylpyridin-5-yl]piperidine-1-carboxylate (Example 80 (3)) (69 mg, 0.225 mmol) and 4-methanesulfonyl-2-methylphenol (48 mg, 0.260 mmol) following a procedure analogous to that in Example 1(3) and (4) as a pale yellow amorphous (37 mg, yield 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536176B2
Source datasetuspto-grants-2013_09
ORD IDord-b5c31a65248e495288e6e39a2ce7696d
Source noteuspto-grants-2013_09