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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685459Generated: October 30, 2026

Diisopropylethylamine → (2R,4R)-1-tert-butyl 2-methyl 4-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)piperidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1685459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant1,4-Benzodioxane-6-carboxylic AcidHCID 2758833—
Reactant(2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylateHCID 54209755—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(2R,4R)-1-tert-butyl 2-methyl 4-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)piperidine-1,2-dicarboxylateHCID 6726641595.1%

Reaction Steps

BOP (6.59 g, 14.9 mmol) was added to a solution of 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid (2.68 g, 14.9 mmol) and DIEA (5.3 mL, 30 mmol) in DMF (50 mL). Then (2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate (3.5 g, 13.5 mmol) was added to the mixture and the resulting solution was stirred at room temperature for 18 hours. Water (100 mL) was added to quench the reaction, and extracted with ethyl acetate (2×100 mL), organic layers were dried over MgSO4, and concentrated under reduced pressure. The residue was purified by Companion (ReadySep, 120 g, silica gel packed) with ethyl acetate/heptane from 20-50% to give the amide as off-white solid 5.4 g (95%). LC-MC: 421.2 (t=2.4 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148401B2
Source datasetuspto-grants-2012_04
ORD IDord-037205d579a942dd9c552d3a234829ba
Source noteuspto-grants-2012_04