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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429578Generated: November 2, 2026

tert-butyl 4-(2-(1-((2-(trimethylsilyl)ethoxy)carbonyl)piperidin-4-yloxy)benzo[d]thiazol-6-yl)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(2-(1-((2-(trimethylsilyl)ethoxy)carbonyl)piperidin-4-yloxy)benzo[d]thiazol-6-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1429578

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(2-(1-((2-(trimethylsilyl)ethoxy)carbonyl)piperidin-4-yloxy)benzo[d]thiazol-6-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 67464645—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(2-(1-((2-(trimethylsilyl)ethoxy)carbonyl)piperidin-4-yloxy)benzo[d]thiazol-6-yl)piperidine-1-carboxylateHCID 6746285669.1%

Reaction Steps

To a solution of tert-butyl 4-(2-(1-((2-(trimethylsilyl)ethoxy)carbonyl)-piperidin-4-yloxy)benzo[d]thiazol-6-yl)-5,6-dihydropyridine-1 (2H)-carboxylate (555 mg, 0.991 mmol) in ethyl acetate (10 mL) was added Pd/C (10%, 2.638 g, 2.48 mmol). The mixture was charged with a balloon of H2 and stirred at rt overnight. The reaction mixture was filtered through a pad of celite and rinsed with EtOAc. The filtrate was concentrated to afford tert-butyl 4-(2-(1-((2-(trimethylsilyl)ethoxy)carbonyl)piperidin-4-yloxy)benzo[d]thiazol-6-yl)piperidine-1-carboxylate (385 mg, 0.685 mmol, 69% yield) as a gray gum. LCMS (m/z)=562 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940716B2
Source datasetuspto-grants-2015_01
ORD IDord-b90ab6d151a84e09b6e4a825a294486c
Source noteuspto-grants-2015_01