HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 118524084, compound → HCID 72943387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 118524084 | HCID 118524084 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 72943387 | HCID 72943387 | 9.1% |
Reaction Steps
Using similar reaction conditions as described in step-ii of example-7, tert-butyl 6-cyclopropyl-3-(1-(3,5-difluorobenzyl)-3,5-dimethyl-1H-pyrazol-4-yl)-5-(4-methoxy-3-(methylsulfonamido)phenyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate (70 mg, 0.103 mmol) was deprotected in HCl in 1,4-dioxane (2 ml). This afforded 5 mg (9.1% yield) of the titled compound. 1H NMR (CD3OD, 300 MHz): δ 8.24 (s, 1H), 7.66 (s, 1H), 7.59-7.58 (m, 1H), 7.38-7.34 (dd, 1H), 7.22-7.19 (m, 1H), 6.93-6.90 (m, 1H), 6.82-6.76 (m, 1H), 5.45-5.39 (t, 2H), 3.96 (s, 3H), 2.94 (s, 3H), 2.5-2.4 (m, 1H), 2.25 (s, 3H), 1.4-1.0 (m, 4H). MS: m/z=538.1 (M+1), HPLC: 81% method B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353107B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-9a108c29e16a4b0296ed8e7b88a4656d |
| Source note | uspto-grants-2016_05 |