HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Oxazol-4-ylmethanamine → HCID 178523064, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Oxazol-4-ylmethanamine | HCID 23055690 | — |
| Reactant | 2-(3-(4-Fluorobenzyl)-2-oxoimidazolidin-1-yl)isonicotinic acid | HCID 58247791 | — |
| Reactant | HCID 178510230 | HCID 178510230 | — |
| Product | HCID 178523064 | HCID 178523064 | 23% |
Reaction Steps
Following the procedure as described in Example 14, making variations as required to replace oxazol-4-ylmethanamine with (1H-pyrazol-3-yl)methanamine to react with 2-(3-(4-fluorobenzyl)-2-oxoimidazolidin-1-yl)isonicotinic acid, N-((1H-pyrazol-3-yl)methyl)-2-(3-(4-fluorobenzyl)-2-oxoimidazolidin-1-yl)isonicotinamide was obtained as a colorless solid in 23% yield: mp 178-180° C.; 1H NMR (300 MHz, CDCl3) δ 8.60 (s, 1H), 8.33-8.24 (m, 2H), 7.45-7.37 (m, 2H), 7.32-7.17 (m, 3H), 7.04-6.94 (m, 2H), 6.27 (s, 1H), 4.70 (d, J=5.7 Hz, 2H), 4.43 (s, 2H), 4.03 (t, J=8.1 Hz, 2H), 3.37 (t, J=8.1 Hz, 2H); MS (ES+) m/z 394.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187426B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-d158313b20a54ee8b64036fc6b813482 |
| Source note | uspto-grants-2015_11 |