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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910929Generated: November 1, 2026

Trifluoroacetic acid → HCID 24825982, compound

https://huagongshe.com/reaction/910929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 24825876HCID 24825876—
SolventDichloromethaneHCID 6344—
ProductHCID 24825982HCID 2482598253.6%

Reaction Steps

A 100 mL round bottom flask was charged with tert-butyl 3-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)piperidine-1-carboxylate (1.65 g, 4.23 mmol) in dichloromethane (10 mL), and 2,2,2-trifluoroacetic acid (0.977 mL, 12.7 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours. A saturated solution of NaHCO3 was added, and the solution was extracted with EtOAc and dichloromethane. The combined organic layers were filtered and concentrated to provide 4-methyl-N-(4-(piperidin-3-yloxy)pyridin-2-yl)thiazol-2-amine as a light yellow solid. (0.70 g, 53.6% yield). Mass spectrum (apci) m/z=291 (100) (+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-69ac81a0964b44dab8497b34434a0c1e
Source noteuspto-grants-2011_09