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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715211Generated: October 30, 2026

1H-Pyrrolo(2,3-b)pyridine → HCID 66725584, compound

https://huagongshe.com/reaction/1715211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
Reactant4-AzaindoleHCID 9226—
ProductHCID 66725584HCID 66725584—

Reaction Steps

Following the procedure as described in PREPARATION 1A, and making non-critical variations using 1H-pyrrolo[3,2-b]pyridine to replace 1H-pyrrolo[2,3-b]pyridine, the title compound was obtained (75%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ 8.39 (d, 1H), 7.56 (d, 1H), 7.25 (d, 1H), 7.05-7.01 (m, 1H), 6.63 (d, 1H), 4.05-3.99 (m, 2H), 1.79-1.72 (m, 2H), 1.31-1.45 (m, 4H), 0.81 (t, 3H); 13C NMR (75 MHz, CDCl3) δ 146.8, 142.9, 131.0, 128.9, 116.5, 116.1, 102.0, 46.6, 30.0, 29.0, 22.2, 14.0; MS (ES+) m/z 189.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799798B2
Source datasetuspto-grants-2010_09
ORD IDord-a3e3cf9300d245fea312bf53ee412e06
Source noteuspto-grants-2010_09