HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 178450287, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178450289 | HCID 178450289 | — |
| Product | HCID 178450287 | HCID 178450287 | 61.4% |
Reaction Steps
Following general procedure A-2, tert-butyl trans-4-[6-(3-chloro-5-fluoro-4-hydroxyphenyl)-3-isobutyrylquinolin-4-ylamino]cyclohexylcarbamate (56 mg, 0.100 mmol) was reacted with TFA (2 mL) to afford the desired product (28 mg, 61%) as a yellow solid: 1H NMR (500 MHz, CD3OD) δ 8.96 (s, 1H), 8.31 (d, J=1.8 Hz, 1H), 7.99 (dd, J=8.7, 1.9 Hz, 1H), 7.90 (d, J=8.7 Hz, 1H), 7.51-7.47 (m, 1H), 7.39 (dd, J=11.8, 2.3 Hz, 1H), 4.23-4.15 (m, 1H), 3.82-3.69 (m, 1H), 3.28-3.18 (m, 1H), 2.39 (d, J=12.7 Hz, 2H), 2.19 (d, J=12.0 Hz, 2H), 1.71 (q, J=10.5 Hz, 2H), 1.62-1.53 (m, 2H), 1.24 (d, J=6.8 Hz, 6H), ESI MS m/z 456[C25H27ClFN3O2+H]+; HPLC 98.1% (AUC), tR=10.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ba9a20c8fc6d46559bae8aec205e752b |
| Source note | uspto-grants-2015_09 |