HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425933Generated: October 30, 2026
HCID 10457822, compound → HCID 10480338, compound
https://huagongshe.com/reaction/425933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10457822 | HCID 10457822 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10480338 | HCID 10480338 | — |
Reaction Steps
To a de-gassed solution of 3-(2,6-dichloro-benzyloxy)-5-[3-(1-methyl-1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indol-5-yl]-pyridin-2-ylamine (example I-61, 130 mg, 0.27 mmol) in methanol (50 mL) and acetic acid (5 mL) was added 10% Pd/C (50 mg). The solution was degassed and charged with hydrogen for three times, and then was stirred under hydrogen balloon for over night. The mixture was filtered through a celite pad, washed with methanol, and then condensed. The residue was dissolved in ethyl acetate, washed with sat. NaHCO3 and brine, dried over Na2SO4, and condensed. The crude product was purified on a silica gel column eluting with dichloromethane-methanol-triethyl amine (95:5:0.1) to provide 3-(2,6-dichloro-benzyloxy)-5-[3-(1-methyl-piperidin-4-yl)-1H-indol-5-yl]-pyridin-2-ylamine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08106197B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-1e8adfe68fa249adb2e857e5bb0147df |
|---|
| Source note | uspto-grants-2012_01 |
|---|