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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184681Generated: November 1, 2026

6-Bromomethyl-4-(3-methylanilino)quinazoline → HCID 22478403, compound

https://huagongshe.com/reaction/2184681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromomethyl-4-(3-methylanilino)quinazolineHCID 22478402—
ReactantHCID 178527776HCID 178527776—
ProductHCID 22478403HCID 2247840359%

Reaction Steps

Using an analogous procedure to that described in Example 34, 6-bromomethyl-4-(3-methylanilino)quinazoline was reacted with 2-mercaptobenzimidazole sodium salt to give 6-(2-benzimidazolylthiomethyl)4-(3-methylanilino)quinazoline in 59% yield, m.p. 123-129° C.; NMR Spectrum: 2.34 (s, 3H), 4.77 (s, 2H), 6.96 (d, 1H), 7.13 (m, 2H), 7.28 (t, 1H), 7.46 (broad s, 2H), 7.68 (m, 3H), 7.96 (m, 1H), 8.57 (s, 1H), 8.65 (d, 1H), 9.79 (broad s, 1H); Elemental Analysis: Found C, 64.9; H, 5.3; N, 15.9; C23H19N5S 1.6H2O 0.1CH3OH requires C, 64.5; H, 5.3; N, 16.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399602B1
Source datasetuspto-grants-2002_06
ORD IDord-24adbd1acf24492c97c10f73d75979fe
Source noteuspto-grants-2002_06