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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234447Generated: October 27, 2026

Diisopropylethylamine → 4-amino-5-chloro-2-fluoro-N-(1-methyl-4-piperidyl)benzamide

https://huagongshe.com/reaction/2234447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant4-Amino-5-chloro-2-fluorobenzoic acidHCID 68683933—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-amino-5-chloro-2-fluoro-N-(1-methyl-4-piperidyl)benzamideHCID 6868246676%

Reaction Steps

4-amino-5-chloro-2-fluorobenzoic acid (Intermediate 176; 500 mg, 2.64 mmol), 4-amino-1-methylpiperidine (452 mg, 3.96 mmol) and diisopropylethylamine (1.38 ml, 7.91 mmol) were stirred in DMF (5 mL) and HATU (1.50 g, 3.96 mmol) added. The reaction mixture was stirred for 3 hours at room temperature. The mixture was absorbed on to an SCX column, which was washed with methanol and eluted with ammonia in methanol. Product containing fractions were concentrated to give a crystalline solid that was suspended in diethyl ether and filtered to yield the title compound as a pale brown solid (572 mg, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709471B2
Source datasetuspto-grants-2010_05
ORD IDord-ac8e82a012ec49d78983a198d8c28bf3
Source noteuspto-grants-2010_05