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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362917Generated: October 25, 2026

Triethylamine → 2-(tert-butoxycarbonyl)amino-5-isopropyl-N-[(1-diphenylmethylpiperidin-4-yl)methyl]benzamide

https://huagongshe.com/reaction/362917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-Aminomethyl-1-diphenylmethylpiperidineHCID 53786046—
Reactant2-{[(Tert-butoxy)carbonyl]amino}-5-(propan-2-yl)benzoic acidHCID 54179894—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(tert-butoxycarbonyl)amino-5-isopropyl-N-[(1-diphenylmethylpiperidin-4-yl)methyl]benzamideHCID 67595919—

Reaction Conditions

Temperature0 °C

Reaction Steps

Step 3): A mixture of 5-isopropyl-N-tert-butoxycarbonylanthranilic acid (1.0 g, 3.58 mmol), 4-aminomethyl-1-diphenylmethylpiperidine (1.0 g, 3.57 mmol), triethylamine (0.37 g, 3.66 mmol) and DPPA (1.0 g, 3.63 mmol) in DMF was stirred at 0° C. for 30 mins and at room temperature for 2 hours. The mixture was poured into H2O and extracted with AcOEt. The extract was washed with H2O, dried over MgSO4 and evaporated and then the residue was purified by column chromatography on silica gel to give 2-(tert-butoxycarbonyl)amino-5-isopropyl-N-[(1-diphenylmethylpiperidin-4-yl)methyl]benzamide, 1.86 g (96.4%): mp 88°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872115
Source datasetuspto-grants-1999_02
ORD IDord-0360362680714b75873f927ddd8e067a
Source noteuspto-grants-1999_02