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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377683Generated: October 31, 2026

Formaldehyde → HCID 10041531, compound

https://huagongshe.com/reaction/2377683

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—
ProductHCID 10041531HCID 10041531—

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 numberUS07470691B2
Source datasetuspto-grants-2008_12
ORD IDord-5b6f6e342f3d415b807a6fb88164844e
Source noteuspto-grants-2008_12