Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374463Generated: October 30, 2026

Trifluoroacetic acid → HCID 58838514, compound

https://huagongshe.com/reaction/2374463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Butoxybenzenesulfonyl ChlorideHCID 517990—
Reactanttert-Butyl (6-aminopyridin-2-yl)carbamateHCID 45092083—
SolventPyridineHCID 1049—
ProductHCID 58838514HCID 58838514—

Reaction Steps

The 4-butoxylphenyl sulfonyl chloride (160 μmol, 2.0 eq, 400 μL of a 0.40 M in anhydrous pyridine) and tert-butyl (6-aminopyridin-2-yl)carbamate (80 μmol, 1.0 eq, 400 μL of a 0.20 M in anhydrous pyridine) was added into a test tube (75×10 mm, dried by heating at 110° C. for 16 h before use) equipped with a stir bar. The test tube was covered with Parafilm, and was stirred for 24 h at ambient temperature. The solvent (pyridine) was evaporated in vacuo. Trifluoroacetic acid (320 μL, 52.0 eq., excess, neat) was added into the test tube. The test tube was capped and vortexed for 5 h at ambient temperature. The excess TFA was removed in vacuo, and the residue was dissolved in DMSO (1.340 mL) and purified by HPLC. 1H NMR (500 MHz, DMSO-d6) δ: 7.73 (d, J=7.7 Hz, 2H), 7.21 (t, J=7.2 Hz, 1H), 6.96 (d, J=6.9 Hz, 1H), 6.10 (d, J=6.1 Hz, 1H), 5.92 (d, J=5.9 Hz, 1H), 3.96 (t, J=6.6 Hz, 1H)), 1.64 (m, 2H), 1.37 (m, 2H), 0.87 (t, J=7.4 Hz, 3H). LRMS m/z: 322.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462634B2
Source datasetuspto-grants-2008_12
ORD IDord-76f1f02bd1fe401aaa7c8d5a02f10a95
Source noteuspto-grants-2008_12