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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945505Generated: November 3, 2026

Diisopropylethylamine → HCID 59605945, compound

https://huagongshe.com/reaction/1945505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2H-Pyran-3(4H)-one, dihydro-HCID 90109—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-(methylamino)piperidine-1-carboxylateHCID 15380702—
SolventDichloromethaneHCID 6344—
ProductHCID 59605945HCID 5960594536.4%

Reaction Steps

A mixture of 4-methylaminopiperidine-1-carboxylic acid tert-butyl ester (200 mg, 0.93 mmol), tetrahydropyran-3-one (187 mg, 1.87 mmol), 4 Å powdered molecular sieves (550 mg) and DIPEA (323 μl, 241 mg, 1.87 mmol) in DCM (10 mL) was stirred at room temperature for 30 min before the addition of sodium triacetoxyborohydride (396 mg, 1.87 mmol). The reaction mixture was stirred at room temperature for 16 h then diluted with DCM and washed with H2O. The organic phase was dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, MeOH:DCM, 0-10%) affording 4-[Methyl(tetrahydropyran-4-yl)amino]piperidine-1-carboxylic acid tert-butyl ester as an oil (101 mg, 36%). 1H NMR (CDCl3, 300 MHz): δ 4.24-4.07 (m, 2 H); 4.06-3.96 (m, 2 H); 3.43-3.32 (m, 2 H); 2.78-2.63 (m, 4 H); 2.25 (s, 3 H); 1.77-1.60 (m, 8 H); 1.46 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-36381ee64ba541329e389eef3f0cb854
Source noteuspto-grants-2013_03