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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554599Generated: October 29, 2026

Benzylamine → HCID 67212258, compound

https://huagongshe.com/reaction/554599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58565108HCID 58565108—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67212258HCID 67212258—

Reaction Steps

3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-bromo-benzoic acid (0.1 g, 0.26 mmol) and catalytic DMF (0.01 mL) were combined in CH2Cl2 (4 mL) at room temperature. Oxalyl chloride (0.03 mL, 0.33 mmol) was added, and the reaction was stirred for 30 minutes. The solution was concentrated and dried under vacuum, and then NMP (3 mL) and diisopropylethylamine (0.14 mL, 0.78 mmol) were added. Benzylamine (0.04 mL, 0.39 mmol) was then added, and the reaction was stirred for 5 minutes. The mixture was poured into H2O and partitioned with 1:1 EtOAc:hexanes. The organic layer was washed with saturated aqueous NaHCO3, H2O, and dilute brine, and then dried, filtered, and concentrated to give N-benzyl-3-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-bromo-benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049015B2
Source datasetuspto-grants-2011_11
ORD IDord-efd90fa628b849328803d7060bcc51ec
Source noteuspto-grants-2011_11