HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-bromoisonicotinate → Methyl 3-[(4-cyanobenzyl)amino]pyridine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-bromoisonicotinate | HCID 2762700 | — |
| Reactant | 4-(Aminomethyl)benzonitrile hydrochloride | HCID 9942250 | — |
| Product | Methyl 3-[(4-cyanobenzyl)amino]pyridine-4-carboxylate | HCID 83335881 | 4% |
Reaction Steps
The title compound was prepared in 4% yield from 4-(aminomethyl)-benzonitrile hydrochloride and methyl 3-bromoisonicotinate according to the procedure for Preparation 4A. 1H NMR (500 MHz, CDCl3): δ 8.07 (s, 1H), 7.97 (d, 2H, J=5.0 Hz), 7.63-7.70 (m, 3H), 7.46 (d, 2H, J=8.3 Hz), 4.61 (d, 2H, J=6.1 Hz), 3.94 (s, 3H). [M+H] calc'd for C15H13N3O2, 268. found 268.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447045B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-0cd2980b2385491d90d66561ce8be405 |
| Source note | uspto-grants-2016_09 |