HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 90033731, compound → HCID 90031293, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 90033731 | HCID 90033731 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hydrochloride methanol | HCID 21893726 | — |
| Product | HCID 90031293 | HCID 90031293 | 70% |
Reaction Steps
Using similar reaction conditions as described in step-ii of example-7, tert-butyl 4-(3-fluoro-5-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridin-2-yl)piperazine-1-carboxylate (125 mg, 0.218 mmol) was deprotected in methanol/HCl in ether (5/2.5 ml) to afford 72 mg (56.2% yield) of the titled compound after purification by prep HPLC. 1H NMR (CD3OD, 300 MHz): δ 8.646-8.640 (d, 1H), 8.56 (s, 1H), 8.419-8.415 (d, 1H), 8.28 (s, 1H), 7.97 (s, 1H), 7.94-7.93 (d, 1H), 7.77 (s, 1H), 7.36-7.33 (m, 1H), 7.11-6.98 (m, 3H), 5.42 (s, 2H), 3.80-3.77 (m, 4H), 3.40-3.31 (m, 4H). MS: m/z=472.3 (M+1), HPLC: 98.87% in method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353107B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-8d178542fc4c41b185946787f9a4254d |
| Source note | uspto-grants-2016_05 |