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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449706Generated: November 1, 2026

Acetic Acid → Tert-Butyl 4-(3-(Isopropylamino)Pyridin-2-Yl)Piperazine-1-Carboxylate

https://huagongshe.com/reaction/1449706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
Reactanttert-Butyl 4-(3-aminopyridin-2-yl)piperazine-1-carboxylateHCID 2756375—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductTert-Butyl 4-(3-(Isopropylamino)Pyridin-2-Yl)Piperazine-1-CarboxylateHCID 10448702—

Reaction Steps

1-[1,1-Dimethylethoxycarbonyl]4-[3-amino-2-pyridinyl]piperazine (International Publication 88/08424, 2.0 g) is dissolved in 35 ml of methanol and acetone (0.48 g) is added. The reaction is cooled to 0° and acetic acid (to pH 4.0) is added. The reaction is stirred 15 min at 0° and then sodium cyanoborohydride (0.50 g) is added. The reaction is allowed to warm slowly to 20-25° and followed by TLC until completion. Additional acetic acid, sodium cyanoborohydride and acetone arc sometimes necessary to force the reaction to completion. The reaction is diluted with chloroform (100 ml), washed with saturated aqueous sodium bicarbonate (50 ml), saline (75 ml), dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography (75 g silica gel, 4:1 hexane/ethyl acetate) affords the title compound, NMR (300 MHz, CDCl3) 7.67, 6.91, 4.15, 3.57, 3.00, 1.48 and 1.23 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599930
Source datasetuspto-grants-1997_02
ORD IDord-2c9ce1e5005e404aa9f2d0fcce020ea4
Source noteuspto-grants-1997_02