HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374463Generated: October 30, 2026
Trifluoroacetic acid → HCID 58838514, compound
https://huagongshe.com/reaction/2374463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Butoxybenzenesulfonyl Chloride | HCID 517990 | — |
| Reactant | tert-Butyl (6-aminopyridin-2-yl)carbamate | HCID 45092083 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 58838514 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462634B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-76f1f02bd1fe401aaa7c8d5a02f10a95 |
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| Source note | uspto-grants-2008_12 |
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