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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410516Generated: October 27, 2026

Sodium Carbonate → Tert-butyl 4-(1-[5-(3-aminophenyl)-1,3-thiazol-2-yl]-1-hydroxyethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/410516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Aminophenylboronic acid monohydrateHCID 14389423—
ReactantTert-butyl 4-[1-(5-bromo-1,3-thiazol-2-yl)-1-hydroxyethyl]piperidine-1-carboxylateHCID 67431988—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductTert-butyl 4-(1-[5-(3-aminophenyl)-1,3-thiazol-2-yl]-1-hydroxyethyl)piperidine-1-carboxylateHCID 6743320792%

Reaction Steps

The product of Step 2 (87 mg, 0.222 mmol), 3-aminophenylboronic acid monohydrate (41.3 mg, 0.267 mmol), Pd(Ph3P)4 (12.85 mg, 0.011 mmol) and Na2CO3 (0.333 mL, 0.667 mmol) were stirred in DME at 100° C. overnight under N2. The reaction mixture was filtered through a pre-pack pad of celica with dichloromethane. The filtrate was concentrated and the residue was purified by flash chromatography to give tert-butyl 4-{1-[5-(3-aminophenyl)-1,3-thiazol-2-yl]-1-hydroxyethyl}piperidine-1-carboxylate (82.4 mg, 0.204 mmol, 92%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-9bbfe7626f7e4124ae0106dfb07abeb6
Source noteuspto-grants-2014_06