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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598821Generated: October 29, 2026

Trifluoroacetic acid → HCID 25175220, compound

https://huagongshe.com/reaction/598821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86635687HCID 86635687—
SolventDichloromethaneHCID 6344—
ProductHCID 25175220HCID 25175220—

Reaction Steps

tert-Butyl(R)-4-(3-(isoquinolin-6-yl)-1,2,4-oxadiazol-5-yl)-1-(4-(trifluoromethyl)phenyl)butan-2-ylcarbamate (0.016 g, 0.03 mmol) was treated with TFA (1 mL, 13 mmol) in 1 mL DCM for 1 hour. After removing the solvent and making the remaining residue basic with 2M ammonia in MeOH, the residue was subjected to a silica gel plug using 3% 2M ammonia in MeOH in DCM as the eluant to yield an off-white solid as the desired product. LCMS (API-ES) m/z (%): 413.0 (100%, M++H); 1H NMR (400 MHz, CD3OD) δ ppm 2.07-2.18 (m, 1H) 2.22 (s, 1H) 2.95-3.03 (m, 1H) 3.05-3.13 (m, 1H) 3.17-3.28 (m, 2H) 3.48-3.58 (m, 1H) 7.52 (d, J=7.53 Hz, 2H) 7.68 (d, J=8.03 Hz, 2H) 7.95 (d, J=5.52 Hz, 1H) 8.23-8.31 (m, 2H) 8.54 (d, J=6.02 Hz, 1H) 8.64 (s, 1H) 9.33 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-a080e1a50d73442ea9b414aa9fc6d524
Source noteuspto-grants-2011_03