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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253446Generated: October 30, 2026

5-Chloro-1H-pyrrolo[2,3-b]pyridine → [2-chloro-6-fluoro-3-(2-methoxy-ethoxy)-phenyl]-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone

https://huagongshe.com/reaction/253446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 24229213—
Reactant2-Chloro-6-fluoro-3-(2-methoxy-ethoxy)-benzaldehydeHCID 59803816—
Reactant[2,6-dichloro-3-(2,2,2-trifluoro-ethoxy)-phenyl]-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-methanolHCID 59803863—
Product[2-chloro-6-fluoro-3-(2-methoxy-ethoxy)-phenyl]-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanoneHCID 24954129—

Reaction Steps

Additional compounds were prepared using the protocol of Scheme 41, optionally substituting 2-chloro-6-fluoro-3-(2-methoxy-ethoxy)-benzaldehyde 123 with a suitable aldehyde (prepared as described in Examples 36, 39 or 40), and/or optionally replacing 5-chloro-1H-pyrrolo[2,3-b]pyridine 4 with an appropriate substituted 7-azaindole (5-methoxy-7-azaindole per Example 8, 5-(1-methyl-1H-pyrazol-4-yl)-7-azaindole per Example 35) in Step 1. The following compounds were made following this procedure:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872018B2
Source datasetuspto-grants-2011_01
ORD IDord-f9bee0ce16a24c73b221395dd71876ff
Source noteuspto-grants-2011_01