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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768351Generated: October 26, 2026

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

https://huagongshe.com/reaction/1768351

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 numberUS07235661B2
Source datasetuspto-grants-2007_06
ORD IDord-333a3562fbe14854824477f4b462a9e7
Source noteuspto-grants-2007_06