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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383891Generated: October 25, 2026

2-Methoxybenzoic acid → Tert-Butyl 3-{[(2-methoxy benzoyl)amino]methyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/383891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxybenzoic acidHCID 11370—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Boc-3-(aminomethyl)piperidineHCID 2756483—
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—
SolventEthyl AcetateHCID 8857—
ProductTert-Butyl 3-{[(2-methoxy benzoyl)amino]methyl}piperidine-1-carboxylateHCID 86649438—

Reaction Steps

HATU (293 mg, 0.77 mmol) was added to a DMF (3 mL) solution of the compound (150 mg, 0.7 mmol) synthesized in (2), 2-methoxybenzoic acid (117 mg, 0.77 mmol), and diisopropylethylamine (0.27 mL, 1.54 mmol), and the mixture was stirred at room temperature for 24 hours. After adding ethyl acetate, the reaction mixture was washed twice with distilled water, and once with saturated brine. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was then purified using silica gel column chromatography to obtain the target (244 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367698B2
Source datasetuspto-grants-2013_02
ORD IDord-3c51d6329d4b4aeeb90928349085ffaa
Source noteuspto-grants-2013_02