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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437185Generated: November 1, 2026

2-Bromoethyl ethyl ether → 4-[1-(2-ethoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1437185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoethyl ethyl etherHCID 61141—
ReactantEthyl 4-(1H-pyrrolo[2,3-b]pyridin-3-yl)piperidine-1-carboxylateHCID 49759051—
Product4-[1-(2-ethoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl esterHCID 68893879101.3%

Reaction Steps

This compound was prepared following the procedure described in example 24, part C, starting with 2.8 g (10 mmol) of 4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid ethyl ester and 1.7 ml (15 mmol) of 2-bromoethylethyl ether. After standard work-up and purification, 3.5 g of 4-[1-(2-ethoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622480B2
Source datasetuspto-grants-2009_11
ORD IDord-1ef51dacdbda43feab135513e1840df3
Source noteuspto-grants-2009_11