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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036828Generated: October 27, 2026

4,6-Dichloro-5-methylpyrimidine → 4-(6-Chloro-5-methyl-pyrimidin-4-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1036828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-5-methylpyrimidineHCID 818860—
Reactanttert-Butyl 4-sulfanylpiperidine-1-carboxylateHCID 21906090—
ReactantSodium t-butoxideHCID 23676156—
SolventTetrahydrofuranHCID 8028—
Product4-(6-Chloro-5-methyl-pyrimidin-4-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 8659736897%

Reaction Steps

A mixture of 4-mercapto-piperidine-1-carboxylic acid tert-butyl ester (1.5352 g, 7.06 mmol) and 4,6-dichloro-5-methyl-pyrimidine (1.1512 g, 7.06 mmol) in 15 mL of THF with sodium t-butoxide (1M in THF, 8.3 mL, 8.3 mmol) added dropwise. After 5 min, mixture was concentrated and residue was extracted with CH2Cl2 and H2O. Organic phase was dried over MgSO4, filtered and concentrated to give 4-(6-chloro-5-methyl-pyrimidin-4-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester as a yellowish solid (2.3469 g, 97%). Exact mass calculated for C15H22ClN3O2S 343.11, found 344.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546429B2
Source datasetuspto-grants-2013_10
ORD IDord-4eb76a977c5642a381950cb5a200623f
Source noteuspto-grants-2013_10