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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835197Generated: November 1, 2026

2-(5-methoxy-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile → 2-(5-Methoxy-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile

https://huagongshe.com/reaction/1835197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-methoxy-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrileHCID 22477215—
Reactant2-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridine-4-carbonitrileHCID 22477322—
SolventEthylacetate heptaneHCID 21899848—
Product2-(5-Methoxy-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrileHCID 22477248—

Reaction Steps

By proceeding in a similar manner to Reference Example 12(a) but using 2-iodo-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile [Reference Example 62(a)] there was prepared the title compound as a yellow solid, m.p. 303-304° C., TLC RF=0.07 (ethyl acetate/heptane 1:1) and 2-(5-methoxy-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile [Reference Example 100] as a brown oil. MS: 443 (MH+). TLC: RF=0.38 (ethyl acetate/heptane 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770643B2
Source datasetuspto-grants-2004_08
ORD IDord-5649b57f65af4b11bfd97d49d306fe1f
Source noteuspto-grants-2004_08