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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822002Generated: October 31, 2026

2,6-Dichloropyridine → HCID 57893630, compound

https://huagongshe.com/reaction/1822002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichloropyridineHCID 16989—
ReactantSodium hydrideHCID 24758—
Reactant1-Piperidinecarboxylicacid,4-hydroxy-2-methyl-,1,1-dimethylethylester,(2S,4S)-(9CI)HCID 45097440—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57893630HCID 57893630—

Reaction Conditions

Temperature65 °C

Reaction Steps

Add sodium hydride (95%, 0.318 g) to a solution of 4-hydroxy-cis-2-methyl-piperidine-1-carboxylic acid tert-butyl ester isomer 2 (preparation 3, 2.465 g) in DMSO (100 mL) and heat in an oil bath at 65° C. After 30 min., add 2,6-dichloropyridine (1.864 g) and beat at 100° C. After 4 hr., partition between ethyl acetate-hexane (1:4) and saturated aqueous NaCl aqueous NaCl, dry over anhydrous sodium sulfate, evaporate and purify on a 35 g silica gel column eluting with ethyl acetate-hexane (1:39) to give the title compound (3.26 g). 1H NMR (CDCl3): 7.50 (t, 1H), 6.87 (d, 1H), 6.61 (d, 1H), 5.38 (m, 1H), 4.35 (m, 1H), 3.89 (m, 1H), 3.22 (m, 1H), 1.93 (m, 3H), 1.75 (m, 1H), 1.46 (s, 9H), 1.26 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608629B2
Source datasetuspto-grants-2009_10
ORD IDord-d15c16a245cf4aedb10224fbf3bed718
Source noteuspto-grants-2009_10