HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81229Generated: October 30, 2026
HCID 178418573, compound → HCID 178467408, compound
https://huagongshe.com/reaction/81229
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178461202 | HCID 178461202 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178467408 | HCID 178467408 | — |
Reaction Steps
To a stirred solution of {6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridin-2-yl}(3-fluoropyridin-2-yl)methanone (618 mg, 1.24 mmol) in THF (10 mL) was added methyl magnesium bromide (3 M in diethyl ether, 0.82 mL, 2.46 mmol) at −78° C., and the reaction mixture was stirred for 2 hours. The reaction mixture was quenched with aqueous saturated NH4Cl solution (40 mL) and extracted with ethyl acetate (2×35 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 (1RS)-1-{6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridin-2-yl}-1-(3-fluoropyridin-2-yl)ethanol. MS APCl calcd. for C26H26Cl2FN5O [M+H]+ 514. found 514.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846657B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-33530c1afd494007b77fb31d251dba05 |
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| Source note | uspto-grants-2014_09 |
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