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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337625Generated: October 29, 2026

Cyclopropylamine → 3,5-dibromo-N-cyclopropyl-4-methylbenzamide

https://huagongshe.com/reaction/337625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Dibromo-4-methylbenzoic acidHCID 670475—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product3,5-dibromo-N-cyclopropyl-4-methylbenzamideHCID 67061951—

Reaction Steps

To a stirred solution of 3,5-dibromo-4-methylbenzoic acid (1 eq.) in DMF (0.4 M) was added HATU (1.3 eq.), cyclopropylamine (1.1 eq.) and Hunig's base (3 eq.). The resulting yellow mixture was stirred at RT for 18 h. The reaction was then quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined organic extracts were washed further with water and brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Trituration of the crude product thus obtained in a mixture of ether and hexanes afforded the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-ea0f3eb7620d419284e644fe8bc865cf
Source noteuspto-grants-2014_11