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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177620Generated: October 30, 2026

Trifluoroacetic acid → HCID 67111566, compound

https://huagongshe.com/reaction/1177620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67111977HCID 67111977—
ReactantHCID 67112045HCID 67112045—
SolventDichloromethaneHCID 6344—
ProductHCID 67111566HCID 67111566—
ProductHCID 67112873HCID 67112873—

Reaction Steps

Separately, the enantiomers of 2-(tert-butoxycarbonylamino)-4-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenyl)butanoic acid were processed by the following procedure: 2-(tert-butoxycarbonyl)-4-(3-fluoro-4-(5-(1-phenylcyclopropyl)-thiazolo[5,4-b]pyridin-2-yl)phenyl)butanoic acid (0.047 g, 0.086 mmol) in DCM (2.0 mL) was added trifluoroacetic acid (1.0 mL, 13 mmol). After 5 min, the solvent was removed, the solid rinsed with water and diethyl ether to give both (R)-2-amino-4-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenyl)butanoic acid trifluoroacetic acid salt and (S)-2-amino-4-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenyl)butanoic acid trifluoroacetic acid salt. MS (ESI) m/z: calculated: 447.1; Observed: 448.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-bdc70a8db66243feb16edd8c10d5fc05
Source noteuspto-grants-2010_11