HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 178507238, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178452630 | HCID 178452630 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178507238 | HCID 178507238 | — |
Reaction Steps
tert-Butyl(E)-2-oxo-3-((3-((E)-2-(pyridin-4-yl)vinyl)-1H-indazol-6-yl)-methyl-ene)indolin-5-ylcarbamate (13 mg, 0.027 mmol) was dissolved into CH2Cl2 (1.0 mL) and then trifluoroacetic acid (0.1 mL) was added and the reaction stirred for 1 hour. The solvent was removed and the residue titurated with ether/EtOAc to give after drying 4.6 mg, 29% of the title compound as an orange powder. 1H NMR (400 MHz, CD3OD) δ 8.68 (d, J=5.8 Hz, 2H), 8.31 (d, J=8.7 Hz, 1H), 8.21-8.12 (m, 3H), 7.97 (s, 1H), 7.88 (s, 1H), 7.70 (d, J=16.8 Hz, 1H), 7.62-7.57 (m, 2H), 7.18 (d, J=8.8 Hz, 1H), 6.99 (d, J=8.6 Hz, 1H); MS ESI 380.1 [M+H]+, calcd for [C23H17N5O+H]+ 380.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765748B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-bce5e83a0be443c6b80790a0b41b8327 |
| Source note | uspto-grants-2014_07 |