HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376141Generated: October 25, 2026
Sodium potassium tartrate tetrahydrate → (5-chloro-6-{[(3R)-1-(cyclohexylmethyl)-3-piperidinyl]amino}-3-pyridinyl)methanol
https://huagongshe.com/reaction/2376141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium potassium tartrate tetrahydrate | HCID 2724148 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | ethyl 5-chloro-6-{[(3R)-1-(cyclohexylmethyl)-3-piperidinyl]amino}nicotinate | HCID 68965163 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-chloro-6-{[(3R)-1-(cyclohexylmethyl)-3-piperidinyl]amino}-3-pyridinyl)methanol | HCID 68961035 | 73.6% |
Reaction Steps
To a stirred solution of ethyl 5-chloro-6-{[(3R)-1-(cyclohexylmethyl)-3-piperidinyl]amino}nicotinate (321 mg) in tetrahydrofuran (6 mL) was added lithium aluminumhydride (80.2 mg) portionwise in an ice bath and the resulting suspension was stirred at the same temperature for three hours. To this was added saturated aqueous potassium sodium (+)-tartrate tetrahydrate solution portionwise at the same temperature and the mixture was stirred at ambient temperature for one hour. The mixture was extracted with ethyl acetate and the aqueous phase was removed. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethylacetate-hexane 1:1 (v/v) to afford (5-chloro-6-{[(3R)-1-(cyclohexylmethyl)-3-piperidinyl]amino}-3-pyridinyl)methanol (210 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465731B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-175889e3555d431b88dd7976e6d80c12 |
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| Source note | uspto-grants-2008_12 |
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