HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Phenylhydroxylamine hydrochloride → 3-(4-Fluorobenzyl)-N-phenoxy-3H-imidazo[4,5-c]pyridine-6-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Phenylhydroxylamine hydrochloride | HCID 6365179 | — |
| Reactant | 3-(4-Fluorobenzyl)-3H-imidazo[4,5-c]pyridine-6-carboxylic acid | HCID 21892227 | — |
| Product | 3-(4-Fluorobenzyl)-N-phenoxy-3H-imidazo[4,5-c]pyridine-6-carboxamide | HCID 10044170 | — |
Reaction Steps
The title compound was prepared by coupling of 3-(4-fluoro-benzyl)-3H-imidazo[4,5-c]pyridine-6-carboxylic acid and N-phenoxyamine hydrochloride under the same conditions as those in step (c) of example 1. 1H NMR (300 MHz, MeOH-d4) δ: 8.82 (s, 1H), 8.53 (s, 1H), 8.43 (s, 1H), 8.24 (d, 2H, J=7.9 Hz), 7.38-7.33 (m, 2H), 7.07-7.01 (m, 2H), 6.88-6.74 (m, 3H), 5.57 (s, 2H). LCMS (API-ES, M+H+): 363.1. HRMS calcd for C20H6FN4O2 (M+H) 363.1257, found 363.1256. HPLC: >85% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368571B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-e5e160f23513486ba16dc8dc9c119918 |
| Source note | uspto-grants-2008_05 |