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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57692Generated: October 26, 2026

Diisopropylethylamine → tert-Butyl 3-({6-[(tert-butoxycarbonyl)amino]-5-(trifluoroacetyl)pyridin-2-yl}amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/57692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-BOC-3-AminopiperidineHCID 545809—
Reactanttert-Butyl[6-chloro-3-(trifluoroacetyl)pyridin-2-yl]carbamateHCID 57911758—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 3-({6-[(tert-butoxycarbonyl)amino]-5-(trifluoroacetyl)pyridin-2-yl}amino)piperidine-1-carboxylateHCID 57911775—

Reaction Conditions

Temperature90 °C

Reaction Steps

561 mg (2.8 mmol) of tert-butyl 3-aminopiperidine-1-carboxylate, 700 mg (2.16 mmol) of tert-butyl [6-chloro-3-(trifluoroacetyl)pyridin-2-yl]carbamate (Example 32A) and 0.56 ml (3.23 mmol) of diisopropylethylamine were suspended in 14 ml of DMSO and heated in a microwave reactor at 90° C. for 45 min. The reaction mixture was diluted with ethyl acetate (100 ml) and washed with saturated aqueous ammonium chloride solution (three times 40 ml) and then saturated aqueous sodium bicarbonate solution (40 ml). The organic phase was dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel (mobile phase: cyclohexane/ethyl acetate 5:1 to 1:1). This gave 670 mg (63% of theory) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434731B2
Source datasetuspto-grants-2016_09
ORD IDord-29e8997d475147c58d94b2780b9537e0
Source noteuspto-grants-2016_09