HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777937Generated: October 31, 2026
(+-)-3-Quinuclidinol → Racemic 6-amino-4-(quinuclidin-3-yloxy)nicotinonitrile
https://huagongshe.com/reaction/1777937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+-)-3-Quinuclidinol | HCID 15381 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 6-Amino-4-fluoronicotinonitrile | HCID 118036901 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Racemic 6-amino-4-(quinuclidin-3-yloxy)nicotinonitrile | HCID 118036915 | — |
Reaction Steps
A solution of KHMDS in THF (1 M, 6.6 ml, 6.60 mmol) was added drop wise to a solution of racemic quinuclidin-3-ol (928 mg, 7.29 mmol) in THF (2 ml) at room temperature. After 55 min a solution of 6-amino-4-fluoronicotinonitrile (intermediate 21, 500 mg, 3.65 mmol) in THF (2 ml) was added and the reaction mixture stirred for 3 days at room temperature. The reaction mixture was partitioned between saturated aqueous NH4Cl and DCM, extracted with DCM (8×), the combined DCM layers were dried over Na2SO4 and evaporated. The residue was preabsorbed onto silica gel and purified by normal phase chromatography with a 12 g RediSep® silica column, eluting with a gradient from DCM to 20% MeOH in DCM. Product containing fractions were combined and evaporated to give the title compound as a beige solid. (UPLC-MS 6) tR 0.32; ESI-MS 245.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266883B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-e6ece83d85674a7784aaef12ea1a3f0a |
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| Source note | uspto-grants-2016_02 |
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