HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221497Generated: October 31, 2026
HCID 10387575, compound → HCID 9999511, compound
https://huagongshe.com/reaction/2221497
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 10387575 | HCID 10387575 | — |
| Reactant | HCID 21892196 | HCID 21892196 | — |
| Product | HCID 9999511 | HCID 9999511 | — |
Reaction Steps
Ethyl 1-(2,4-difluorobenzyl)-5-formyl-1H-pyrrolo[2,3-c]pyridine-2-carboxyl ate. The title compound can be prepared by alkylation of ethyl 5-formyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylate (prepared according to J.-F. Rousseau, R. H. Dodd, X. Doisy, P. Potier, Heterocycles 1989, 28, 1101-1113) and 2,4-difluorobenzyl bromide in a manner similar to step (a) in Example 1. (b) 1-(2,4-Difluorobenzyl)-(2-ethoxycarbonyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid. The title compound can be prepared by oxidation of ethyl 1-(2,4-difluoro-benzyl)-5-formyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylate according to the procedure by R. H. Dodd, M. Le Hyaric, Synthesis 1993, 295-287. (c) Ethyl 1-(2,4-Difluorobenzyl)-5-hydroxycarbamoyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylate. The title compound can be prepared from 1-(2,4-difluorobenzyl)-(2-ethoxycarbonyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid following in a manner similar to step (c ) in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368571B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-7f08f5acfafa4b8584eff33f5ae106e1 |
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| Source note | uspto-grants-2008_05 |
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