HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Cyanopropyloxy)benzoic acid → 4-(3-cyanopropoxy)-N-[4-(5-cyano-3-pyridin-3-yl-pyrazol-1-yl)phenyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Cyanopropyloxy)benzoic acid | HCID 14650336 | — |
| Reactant | 1-(4-Aminophenyl)-3-(3-pyridyl)-5-cyanopyrazole | HCID 18677106 | — |
| Product | 4-(3-cyanopropoxy)-N-[4-(5-cyano-3-pyridin-3-yl-pyrazol-1-yl)phenyl]benzamide | HCID 9803703 | — |
Reaction Steps
The 4-(cyanopropyloxy)benzoic acid (0.75 mmol) was coupled with 3-(3-pyridyl)-5-cyano-1-(4′-aminophenyl)-pyrazole (0.5 mmol) under standard EDC mediated conditions (Method A). The crude product was recrystallized from hot benzene/methanol, m.p. 193-194° C. 1H NMR(CDCl3): δ 2.04-2.11 (m, 2H), 2.68-2.71 (7, J=7.1 Hz, 2H), 4.14-4.17 (t, J=6 Hz, 2H), 7.11-7.13 (d, J=8.6 Hz, 2H), 7.53-7.56 (m, 1H), 7.79-7.82(d, J=8.7 Hz, 2H), 8.00-8.05 (m, 4H), 8.1 (s, 1H), 8.30-8.32 (d, J=8 Hz, 1H), 8.63-8.64(d, J=4.6 Hz, 1H), 9.15 (s, 1H), 10.4 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506747B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-bdfa8440a492474e9ec2851b3b41de09 |
| Source note | uspto-grants-2003_01 |