HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Isopropylhydroxylamine Hydrochloride → 1-(4-Fluorobenzyl)-N-hydroxy-N-isopropyl-1H-pyrrolo[2,3-c]pyridine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Isopropylhydroxylamine Hydrochloride | HCID 170873 | — |
| Reactant | 1-(4-fluorobenzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid | HCID 21892207 | — |
| Product | 1-(4-Fluorobenzyl)-N-hydroxy-N-isopropyl-1H-pyrrolo[2,3-c]pyridine-5-carboxamide | HCID 11667020 | — |
Reaction Steps
The title compound was prepared by coupling of 1-(4-fluorobenzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid with N-isopropyl hydroxylamine hydrochloride in a manner similar to step 8 of example 1. 1H NMR (CDCl3) δ ppm 8.59 (s, 1H), 8.46 (s, 1H), 7.39 (s, 1H), 7.10 (m, 2H), 7.02 (d, 2H, J=8.6 Hz), 6.73 (s, 1H), 5.41 (s, 2H), 5.08 (m, 1H), 1.33 (d, 6H, J=6.6 Hz). LCMS (APCI, M+H+): 328.1 HRMS calcd for C18H18FN3O2 (M+H) 328.1456, found 328.1456. HPLC: 95.8% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468375B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-df3304d45e0342cb9c6f37b027df479d |
| Source note | uspto-grants-2008_12 |