HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-(1H-1,2,3,4-tetrazol-5-yl)phenyl)methanamine hydrochloride → 5-Fluoro-2-(4-fluorobenzyl)-N-[4-(2H-tetrazol-5-YL)benzyl]nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-(1H-1,2,3,4-tetrazol-5-yl)phenyl)methanamine hydrochloride | HCID 23224690 | — |
| Reactant | 5-Fluoro-2-(4-fluorobenzyl)nicotinic acid | HCID 57572265 | — |
| Product | 5-Fluoro-2-(4-fluorobenzyl)-N-[4-(2H-tetrazol-5-YL)benzyl]nicotinamide | HCID 58905382 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 75 from 5-fluoro-2-(4-fluorobenzyl)nicotinic acid (step 3 of Example 58) and 1-[4-(2H-tetrazol-5-yl)phenyl]methanamine hydrochloride: 1H-NMR (DMSO-d6) δ 9.20 (1H, t, J=5.7 Hz), 8.59 (1H, d, J=2.8 Hz), 7.98 (2H, d, J=8.1 Hz), 7.83 (1H, dd, J=8.8, 2.9 Hz), 7.44 (2H, d, J=8.1 Hz), 7.20–7.16 (2H, m), 7.03 (2H, t, J=8.9 Hz), 4.50 (2H, d, J=5.7 Hz), 4.21 (2H, s); MS (ESI) m/z 407 (M+H)+, 405 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238714B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-170da0dc45d44d4a92a440a7011b4dff |
| Source note | uspto-grants-2007_07 |