HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-Hydroxyadamantan-1-yl)acetic acid → 2-(3-hydroxyadamantan-1-yl)-N-(4-isopropyl-1-oxophthalazin-2(1H)-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-Hydroxyadamantan-1-yl)acetic acid | HCID 429307 | — |
| Reactant | 2-amino-4-isopropylphthalazin-1(2H)-one | HCID 67161646 | — |
| Product | 2-(3-hydroxyadamantan-1-yl)-N-(4-isopropyl-1-oxophthalazin-2(1H)-yl)acetamide | HCID 67160060 | — |
Reaction Steps
The product of Example 1B and 2-(3-hydroxyadamantan-1-yl)acetic acid were processed using a method similar to that described in Example 17C to afford the title compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 11.12 (s, 1H), 8.34 (dd, J=7.9, 1.3 Hz, 1H), 8.11 (d, J=8.1 Hz, 1H), 8.00 (ddd, J=8.3, 7.1, 1.3 Hz, 1H), 7.89 (ddd, J=8.0, 7.1, 1.0 Hz, 1H), 3.61 (p, J=6.7 Hz, 1H), 2.08-2.11 (m, 4H), 1.36-1.63 (m, 13H), 1.26 (d, J=6.7 Hz, 6H); MS (ESI) m/z 396 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629143B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-c97e7ec9999b4051ab865b179a5cae1e |
| Source note | uspto-grants-2014_01 |