HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 178509552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178454011 | HCID 178454011 | — |
| Product | HCID 178509552 | HCID 178509552 | 67.4% |
Reaction Steps
Following general procedure A-2, tert-butyl trans-4-[6-(5-cyanothiophen-2-yl)-3-(cyclopropane carbonyl)quinolin-4-ylamino]cyclohexylcarbamate (24 mg, 0.047 mmol) was reacted with TFA (2 mL) to afford the desired product (13.2 mg, 32%) as a yellow solid: 1H NMR (500 MHz, CD3OD) δ 9.25 (s, 1H), 8.54 (s, 1H), 8.27 (d, J=8.6 Hz, 1H), 7.98 (d, J=8.8 Hz, 1H), 7.85 (d, J=4.0 Hz, 1H), 7.70 (d, J=4.0 Hz, 1H), 4.28 (s, 1H), 3.28-3.25 (m, 1H), 2.89-2.83 (m, 1H), 2.42 (d, J=12.8 Hz, 2H), 2.23 (d, J=12.2 Hz, 2H), 1.80-1.63 (m, 4H), 1.27-1.21 (m, 2H), 1.19-1.13 (m, 2H); ESI MS m/z 417 [C24H24N4OS+H]+; HPLC 95.1% (AUC), tR=10.32 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-2d0c4a0788a045c3af1de02b4b471468 |
| Source note | uspto-grants-2015_09 |