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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643706Generated: October 30, 2026

Pivaloyl chloride → N-(5-Bromo-2-{[(1-hydroxycyclopentyl)methyl]amino}phenyl)-2,2-dimethylpropanamide

https://huagongshe.com/reaction/643706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 65103218HCID 65103218—
SolventEthyl AcetateHCID 8857—
ProductN-(5-Bromo-2-{[(1-hydroxycyclopentyl)methyl]amino}phenyl)-2,2-dimethylpropanamideHCID 6861475884.8%

Reaction Steps

To a solution of 1-([(2-amino-4-bromophenyl)amino]methyl)cyclopentanol (Step B, 1.3 g, 4.15 mmol) in ethyl acetate (100 mL) was added pivaloyl chloride (511 mg, 4.15 mmol) at room temperature. After stirring for 2 h at room temperature, the mixture was quenched with saturated sodium hydrogen carbonate aqueous solution. The mixture was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1 as eluent) to afford the title compound (1.3 g, 75%) as a beige amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700618B2
Source datasetuspto-grants-2010_04
ORD IDord-2b76ea0856494de0aaeecb946f5be987
Source noteuspto-grants-2010_04