HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4'-piperidin]-4-one → HCID 178488445, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4'-piperidin]-4-one | HCID 57519244 | — |
| Reactant | HCID 178488446 | HCID 178488446 | — |
| Product | HCID 178488445 | HCID 178488445 | — |
Reaction Steps
The compound is synthesized according to the procedure described in Example 1, using 6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4′-piperidin]-4-one instead of 4-oxospiro(chroman-2,4′-piperidin)-6-yl acetamide, and 8-methoxy-4-(1H-tetrazol-5-yl)-2-naphthoic acid instead of 4,8-dimethoxyquinoline-2-carboxylic acid. 1H-NMR (400 MHz, DMSO-d6) δ: 8.39 (1H, s), 8.21 (1H, d, J=8.0 Hz), 8.12 (1H, s), 8.01 (1H, d, J=2.0 Hz), 7.83-7.77 (3H, m), 7.63 (1H, t, J=8 Hz), 7.15 (1H, d, J=8 Hz), 7.11 (1H, d, J=8.0 Hz), 4.40-4.22 (1H, m), 4.02 (3H, s), 3.83 (3H, s), 3.70-3.30 (3H, m), 2.89 (2H, s), 2.12-1.75 (4H, m). MS [M+H]+=550.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935712B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-285e9347d1564f29b38c948558c701cb |
| Source note | uspto-grants-2011_05 |