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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307998Generated: November 2, 2026

Cyanogen Bromide → N7-(1-Ethyl-propyl)-5-methyl-3-(2,4,6-trimethyl-phenyl)-3H-imidazo[4,5-b]pyridine-2,7-diamine

https://huagongshe.com/reaction/2307998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantN4-(1-ethyl-propyl)-6-methyl-N2-(2,4,6-trimethyl-phenyl)-pyridine-2,3,4-triamineHCID 21912187—
SolventAcetonitrileHCID 6342—
ProductN7-(1-Ethyl-propyl)-5-methyl-3-(2,4,6-trimethyl-phenyl)-3H-imidazo[4,5-b]pyridine-2,7-diamineHCID 21912344—

Reaction Steps

The title compound was prepared by reacting N4-(1-ethyl-propyl)-6-methyl-N2-(2,4,6-trimethyl-phenyl)-pyridine-2,3,4-triamine with BrCN in acetonitrile at room temperature overnight. The mixture was quenched with water and adjusted to pH 8.0 with saturated sodium bicarbonate and extracted with ethyl acetate. The organic layer was separated, dried and concentrated to give crude material. The material was purified through silica gel column chromatography to give the title compound as a brown solid, mp. 158-160° C.; Anal. For C21H29N5 ¼H2O calc. C, 70.85; H, 8.35; N, 19.67; found: C, 71.07; H, 8.30; N, 19.63.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833378B2
Source datasetuspto-grants-2004_12
ORD IDord-1aca15a54bed47e9b871fff5c81e43ed
Source noteuspto-grants-2004_12