HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822002Generated: October 31, 2026
2,6-Dichloropyridine → HCID 57893630, compound
https://huagongshe.com/reaction/1822002
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dichloropyridine | HCID 16989 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Piperidinecarboxylicacid,4-hydroxy-2-methyl-,1,1-dimethylethylester,(2S,4S)-(9CI) | HCID 45097440 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57893630 | HCID 57893630 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608629B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-d15c16a245cf4aedb10224fbf3bed718 |
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| Source note | uspto-grants-2009_10 |
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