Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497159Generated: October 26, 2026

Hydrochloric Acid → 1H-Pyrrolo[2,3-b]pyridine-4-carbaldehyde

https://huagongshe.com/reaction/497159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium BicarbonateHCID 516892—
Reactant1H-pyrrolo(2,3-b)pyridine-4-carbonitrileHCID 11715196—
ReactantDibahHCID 16682954—
SolventTetrahydrofuranHCID 8028—
Product1H-Pyrrolo[2,3-b]pyridine-4-carbaldehydeHCID 2196388752%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (200 mg, 1.4 mmol) of 1H-Pyrrolo[2,3-b]pyridine-4-carbonitrile in THF (7 mL) at −78° C. under nitrogen was added Dibal-H (1.0 M in toluene, 3.07 mL, 3.07 mmol). The reaction mixture was stirred at −78° C. for 1 hr, warmed to 55° C. and stirred for additional 2 hr. One additional equivalent of DIBAL-H (1.4 mL, 1.4 mmol) was added and the mixture stirred at 55° C. for 2 hr. The mixture was cooled to 5° C., acidified with 2 M HCl and stirred for 15 min. The mixture was then neutralized with saturated NaHCO3 (aq), extracted with CH2Cl2 (5×25 mL), washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give 1H-Pyrrolo[2,3-b]pyridine-4-carboxaldehyde (107 mg, 52%). MS (ES+): 146 [MH+]. 1H NMR (DMSO-d6, 400 MHz): δ 7.22 (d, 1H, J=3.6 Hz), 7.57 (d, 1H, J=4.8 Hz), 7.67 (d, 1H, J=2.4 Hz), 8.61 (d, 1H, J=5.2 Hz), 10.42 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949563B2
Source datasetuspto-grants-2005_09
ORD IDord-83bffc2d0a1046e09f4d27f532478116
Source noteuspto-grants-2005_09