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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828281Generated: October 26, 2026

Formaldehyde → 2-[4-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-1-piperazinyl]benzonitrile

https://huagongshe.com/reaction/1828281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
ReactantN-(2-Cyanophenyl)piperazineHCID 2735875—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-[4-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-1-piperazinyl]benzonitrileHCID 22065975—

Reaction Steps

1H-pyrrolo[2,3-b]pyridine (47 mg, 0.40 mmol), 2-(1-piperazinyl)benzonitrile (65 mg, 0.48 mmol), sodium acetate (72 mg, 0.53 mmol), and formaldehyde (0.48 mmol) were combined in water and glacial acetic acid (1:2, 1 mL) and stirred at room temperature for 18 hours. The mixture was treated with a solution of 2M NaOH and concentrated under reduced pressure. The residue was treated with hot methanol. The methanol was filtered and the filter cake was washed with cold methanol to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ 2.62 (m, 4H) 3.14 (m, 4H) 4.03 (s, 2H) 5.60 (s, 1H) 7.09 (m, 3H) 7.61 (m, 2H) 8.06 (dd, J=8.31, 1.53 Hz, 1H) 8.20 (dd, J=4.75, 1.70 Hz, 1H). (ESI) m/z 318 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057042B2
Source datasetuspto-grants-2006_06
ORD IDord-4c9b147ce2554be5a7ada2279ad49f83
Source noteuspto-grants-2006_06