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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273328Generated: October 30, 2026

6-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine → 6-Methyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/273328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 49759033—
ReactantHCID 178477797HCID 178477797—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product6-Methyl-1H-pyrrolo[2,3-b]pyridineHCID 1145771688%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methylzinc chloride in THF (2 M) (9 mL, 12 mmol) was added to 6-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (0.600 g, 2.05 mmol) and Pd(PPh3)4 (0.095 g, 0.08 mmol) in THF (30 mL). The mixture was refluxed for 40 h, cooled to 0° C., quenched with water and extracted with Et2O. The organic layer was concentrated and the residue was purified over a silica gel column eluting with EtOAc/hexane (1:5) to give N-protected 6-methyl-7-azaindole (0.495 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456289B2
Source datasetuspto-grants-2008_11
ORD IDord-e565e8d0101240769f247e2833515134
Source noteuspto-grants-2008_11