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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203174Generated: October 31, 2026

methyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylate → 1-(5-Chloro-1-isobutyl-1H-indazol-7-ylmethyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/2203174

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 22832049—
Reactant(5-Chloro-1-isobutyl-1H-indazole-7-yl)-methanolHCID 118251601—
Product1-(5-Chloro-1-isobutyl-1H-indazol-7-ylmethyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl esterHCID 11825164873%

Reaction Steps

Compound 36 was prepared following general method 3A, using compound 17 as a starting material and 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester as the heterocycle. Yield: 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365569B2
Source datasetuspto-grants-2016_06
ORD IDord-cf53901f5c74429e8c12d203a9c9d760
Source noteuspto-grants-2016_06