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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177563Generated: October 27, 2026

Trifluoroacetic acid → 3-(3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenylamino)propanoic acid

https://huagongshe.com/reaction/1177563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 3-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenylamino)-propanoateHCID 67111760—
SolventDichloromethaneHCID 6344—
Product3-(3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenylamino)propanoic acidHCID 44599686—

Reaction Conditions

Temperature25 °C

Reaction Steps

2,2,2-Trifluoroacetic acid (360 μl, 4.67 mmol) was added to a solution of tert-butyl 3-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenylamino)propanoate (46.5 mg, 0.095 mmol) in DCM (2.0 mL) at 25° C., and the resulting solution was stirred at 25° C. for 19 h. The reaction solution was then concentrated in vacuo, and the residue was taken up in DMSO (2.0 mL) and purified by rpHPLC (10-100% CH3CN/water+0.1% TFA) to provide 3-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenylamino)propanoic acid as a yellow solid. MS (ESI) m/z: Calculated: 433.1; Observed: 434.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-d0274c306fcc4982a756931ec6c82743
Source noteuspto-grants-2010_11