HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852833Generated: October 25, 2026
3-Fluoro-2-pyridinecarboxaldehyde → HCID 178461203, compound
https://huagongshe.com/reaction/1852833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoro-2-pyridinecarboxaldehyde | HCID 11344017 | — |
| Reactant | HCID 178424953 | HCID 178424953 | — |
| Reactant | HCID 178461250 | HCID 178461250 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178461203 | HCID 178461203 | — |
Reaction Steps
To a stirred solution of 6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine (Preparative Example 3.1, Step 1) (1.2 g, 3.19 mmol) in THF (20 mL) was added 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex (Aldrich, 1M in THF/toluene) (5.11 mL, 5.11 mmol) at −78° C., and the reaction was stirred at −78° C. for 2 hours under a nitrogen atmosphere. 3-fluoropicolinaldehyde (1.1 g, 9.59 mmol) dissolved in THF (4.0 mL) was added dropwise at −78° C., and the reaction was stirred for an additional 2 hours at −78° C. The reaction was quenched with aqueous saturated NH4Cl solution (50 mL) and extracted with ethyl acetate (2×40 mL). The combined organic extracts were washed with brine (20 mL), dried over anhydrous Na2SO4, filtered, and concentrated. Purification of the residue on a silica gel column (0 to 100% EtOAc/hexanes) afforded {6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridin-2-yl}(3-fluoropyridin-2-yl)methanol. MS APCI calcd. for C25H24Cl2FN5O [M+H]+ 500. found 500.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962611B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-ba27135120f6456d9ff1dba370809d14 |
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| Source note | uspto-grants-2015_02 |
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