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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821907Generated: November 1, 2026

HCID 11217626, compound → 7-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carbaldehyde

https://huagongshe.com/reaction/1821907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11217626HCID 11217626—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product7-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carbaldehydeHCID 5789356486.4%

Reaction Steps

A mixture of (7-chloro-1H-pyrrolo[2,3-c]pyridin-2-yl)methanol (Example 1) (2.81 g, 15.4 mmol), manganese(IV)oxide (16 g) and dichloromethane (250 mL) was stirred under an atmosphere of nitrogen for 16 h. The mixture was filtered through a pad of diatomaceous earth, washing generously with hot acetone. Evaporation of the solvents provided 7-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde (2.40 g, 13.3 mmol, 84%) as a mixture of aldehyde and aldehyde hydrate: 1H NMR (300 MHz, CD3OD) δ5.79 (1H, s), 6.65 (1H, s), 7.44 (1H, s), 7.53 (1H, d, J=5.5 Hz), 7.72 (1H, d, J=5.5 Hz), 7.85 (1H, d, J=5.5 Hz), 7.99 (1H, d, J=5.5 Hz), 10.02 (1H, s); ESI MS m/z 181 [C8H5ClN2O+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608627B2
Source datasetuspto-grants-2009_10
ORD IDord-822f00288f664837995491054ad02b8e
Source noteuspto-grants-2009_10