HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422559Generated: October 26, 2026
(S)-2-(1-{[2-chloro-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1,1,1-trifluorobutan-2-ol → (S)-2-(1-{[2-cyclopropyl-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1,1,1-trifluorobutan-2-ol
https://huagongshe.com/reaction/2422559
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-2-(1-{[2-chloro-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1,1,1-trifluorobutan-2-ol | HCID 86621982 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-(1-{[2-cyclopropyl-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1,1,1-trifluorobutan-2-ol | HCID 66790907 | — |
Reaction Steps
To a solution of (S)-2-(1-{[2-chloro-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1,1,1-trifluorobutan-2-ol (100 mg, 0.22 mmol) in THF (3 mL) was added Ni(dppp)Cl2 (12 mg, 0.02 mmol) and cyclopropylmagnesium bromide (0.5M, 1.3 mL, 0.66 mmol). The mixture was stirred at 60° C. for 2 h. The reaction was quenched with saturated aqueous NH4Cl and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduce pressure. Purification on silica gel (eluting with acetone/dichloromethane, 1:9) gave the title compound MS (+ESI): 471 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960409B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-5f18236c70ab466583f35a0667bdae0a |
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| Source note | uspto-grants-2011_06 |
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