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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091623Generated: November 2, 2026

O-Phenylenediamine → 2-[1H-benzimidazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetonitrile

https://huagongshe.com/reaction/1091623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
Reactant3,3-Bis(methylthio)-2-(pyrimidin-2-yl)acrylonitrileHCID 59268208—
Product2-[1H-benzimidazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetonitrileHCID 66593256—
ProductHCID 66593501HCID 66593501—

Reaction Steps

In the first step of the synthesis, a benzene-1,2-diamine (1, X═NH) or 2-aminothiophenol (1, X═S) is coupled with a 3,3-bis(methylthio)-2-(pyrimidin-2-yl)acrylonitrile 9 to give a 2-[1H-benzimidazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetonitrile or 2-[benzothiazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetonitrile 6. The reaction is carried out under generally the same conditions as are used in the first step of the first half of Reaction Scheme 1. In the second step, the compound of formula 6 is hydrolyzed to a 2-[1H-benzimidazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetamide or 2-[benzothiazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetamide 8, as in Reaction Scheme 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129396B2
Source datasetuspto-grants-2012_03
ORD IDord-3c716cd7d49e4fd8946d26b4e248cd3e
Source noteuspto-grants-2012_03