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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628018Generated: November 1, 2026

Cyclohexylamine → HCID 58382222, compound

https://huagongshe.com/reaction/1628018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantHCID 58382073HCID 58382073—
ProductHCID 58382222HCID 5838222248.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 4-chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (1.5 g, 3.9 mmol) and cyclohexylamine (2.34 g, 23.6 mmol) was stirred at about 80° C. for about 24 h. The solvent was removed under reduced pressure. The residue was suspended in Et2O and the precipitate was collected by filtration and dried under vacuum. The solid was washed with water and dried under vacuum again to give ethyl-4-(cyclohexylamino)-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (0.54 g, 48%): LC/MS (Table 2, Method b) Rt=2.56 min.; MS m/z: 288 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785639B2
Source datasetuspto-grants-2014_07
ORD IDord-e29aa407bd574a2fa11ef5049ccafbc9
Source noteuspto-grants-2014_07