HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047572Generated: October 31, 2026
HCID 178418361, compound → HCID 178429874, compound
https://huagongshe.com/reaction/1047572
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178429876 | HCID 178429876 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178429874 | HCID 178429874 | 71.1% |
Reaction Steps
2-Methyl-4-(2-(5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-3-yl)-1H-benzo[d]imida-zol-5-yl)morpholine (60 mg, 0.130 mmol) was added to 10% Pd/C (10 mg) in ethanol (25 mL) and then hydrogen gas (60 psi) was applied for 8 h at room temperature. The reaction mixture was filtered through Celite, and the solvent was removed in vacuo. Purification by flash chromatography (5% CH3OH/CH2Cl2) afforded the title compound (40 mg). 1H NMR: (400 MHz, CD3OD): δ 7.66 (d, 1H, J=2.0 Hz), 7.52 (m, 2H), 7.13 (s, 1H), 7.04-7.00 (m, 2H), 5.79 (dd, 1H, J=2.4 and 9.2 Hz), 3.97 (m, 2H), 3.79 (m, 3H), 3.49 (m, 1H), 3.41 (m, 1H), 2.76 (m, 1H), 2.62 (m, 1H), 2.44 (m, 1H), 2.13 (m, 1H), 2.05 (m, 1H), 1.80 (m, 1H), 1.68 (m, 2H), 1.22 (d, 3H, J=6.4 Hz); ESI-MS [M+H]+: 433.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569511B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-1d08b49987d34363ad6075990900c83a |
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| Source note | uspto-grants-2013_10 |
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