HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 118524099, compound → HCID 90064831, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 118524099 | HCID 118524099 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 90064831 | HCID 90064831 | 50.1% |
Reaction Steps
Using similar reaction conditions as described in step-ii of example-7, tert-butyl 4-(3-(3-(1-(3-fluorobenzyl)-3,5-dimethyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-5-yl)benzyl)piperidine-1-carboxylate (60 mg, 0.101 mmol) was deprotected in HCl in methanol (5 ml). This afforded 25 mg (40.6% yield) of the titled compound. 1H NMR (CD3OD, 400 MHz): δ 8.67 (s, 1H), 8.34 (s, 1H), 7.66 (s, 1H), 7.56-7.54 (m, 2H), 7.48-7.38 (m, 2H), 7.30-7.28 (d, 1H), 7.08-7.04 (m, 2H), 6.93-6.91 (d, 1H), 5.42 (s, 2H), 3.40-3.37 (d, 2H), 2.98-2.92 (t, 2H), 2.74-2.72 (d, 2H), 2.25-2.23 (d, 6H), 2.10-1.90 (m, 3H), 1.53-1.47 (m, 2H). MS: m/z=494.3 (M+1), HPLC: 95.16% in method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353107B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-36a8036c500b49329959c470a7285d40 |
| Source note | uspto-grants-2016_05 |