HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → 3'-(7-Hydroxyiminomethylimidazo [1,2-alpha]pyridin-3-yl)biphenyl-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3'-(7-Formylimidazo[1,2-alpha]pyridin-3-yl)biphenyl-2-carbonitrile | HCID 9858378 | — |
| Product | 3'-(7-Hydroxyiminomethylimidazo [1,2-alpha]pyridin-3-yl)biphenyl-2-carbonitrile | HCID 136473467 | — |
Reaction Steps
The title compound was prepared in a similar manner to that described in Example 14 using hydroxylamine hydrochloride (77 mg, 1.11 mmol) and 3′-(7-formylimidazo[1,2-α]pyridin-3-yl)biphenyl-2-carbonitrile (120 mg, 0.37 mmol) to afford a white crystalline solid (105 mg, 83%), essentially as a single geometric isomer. 1H NMR (400 MHz, d6-DMSO) δH 7.27 (1H, dd, J 1 and 7), 7.61-7.90 (8H, m), 7.90 (2H, s), 8.00 (1H, dd, J 8 and 1), 8.25 (1H, s), 8.68 (1H, d, J 7), 11.53 (1H, s); m/z (ES+) 339 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872731B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-908f52ebd1454fab8feffeecccbebb7b |
| Source note | uspto-grants-2005_03 |