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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250929Generated: November 1, 2026

Diisopropylamine → furan-3-carboxylic acid N'-[2-(5-fluoro-2'-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N'-isopropyl-hydrazide

https://huagongshe.com/reaction/2250929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPyBroPHCID 2733179—
Reactant(5-Fluoro-2'-trifluoromethoxy-biphenyl-2-yloxy)-acetic acidHCID 58689904—
Reactantfuran-3-carboxylic acid N'-isopropyl-hydrazideHCID 58689920—
SolventDimethylformamideHCID 6228—
Productfuran-3-carboxylic acid N'-[2-(5-fluoro-2'-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N'-isopropyl-hydrazideHCID 1167735756%

Reaction Steps

A solution of (5-fluoro-2′-trifluoromethoxy-biphenyl-2-yloxy)-acetic acid (180 mg, 0.54 mmol) and furan-3-carboxylic acid N′-isopropyl-hydrazide (110 mg, 0.65 mmol) in DMF (5 ml) was treated with diisopropyl amine (0.237 ml, 1.36 mmol) and PyBroP (381 mg, 0.82 mmol) at room temperature overnight. The reaction mixture was partitioned between 1N HCl and ethyl acetate. The organic layer was successively washed with aqueous saturated sodium bicarbonate and brine, then dried over sodium sulfate, filtered and concentrated. The crude was absorbed on silica and purified on a silica gel column with a 30-50% ethyl acetate in hexanes gradient to afford the product as a solid (145 mg, 56%). MS m/e 481.35 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317125B2
Source datasetuspto-grants-2008_01
ORD IDord-c7a937ea4c3046319ebb7ec8397a0c93
Source noteuspto-grants-2008_01