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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946372Generated: October 27, 2026

1-Heptanol, 7-bromo- → N-[1-({2-Chloro-4-[(7-hydroxyheptyl)oxy]phenyl}methyl)-1H-pyrazol-3-yl]-2,6-difluorobenzamide

https://huagongshe.com/reaction/1946372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Heptanol, 7-bromo-HCID 66284—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-{1-[(2-Chloro-4-hydroxyphenyl)methyl]-1H-pyrazol-3-yl}-2,6-difluorobenzamideHCID 59547950—
SolventDimethyl SulfoxideHCID 679—
SolventAcetonitrileHCID 6342—
ProductN-[1-({2-Chloro-4-[(7-hydroxyheptyl)oxy]phenyl}methyl)-1H-pyrazol-3-yl]-2,6-difluorobenzamideHCID 59547851—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N-{1-[(2-chloro-4-hydroxyphenyl)methyl]-1H-pyrazol-3-yl}-2,6-difluorobenzamide (for a preparation see Example 31)(30 mg, 0.082 mmol) in acetonitrile (0.5 ml) was added potassium t-butoxide (9.4 mg, 0.084 mmol) and then 7-bromo-1-heptanol (0.015 ml, 0.099 mmol, Aldrich). The reaction vessel was sealed and heated in a Biotage Initiator microwave to 100° C. for 15 min. After cooling the reaction was diluted with DMSO (0.5 ml) and purified by MDAP on Sunfire C18 column using Acetonitrile-Water with a Formic acid modifier (Method B). The solvent was evaporated in vacuo to give the title compound as a colourless gum (6.7 mg);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-115d4f7805dc4d5badd51f599480d2ab
Source noteuspto-grants-2013_03