HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromomethyl-4-(3-methylanilino)quinazoline → HCID 22478403, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromomethyl-4-(3-methylanilino)quinazoline | HCID 22478402 | — |
| Reactant | HCID 178527776 | HCID 178527776 | — |
| Product | HCID 22478403 | HCID 22478403 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399602B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-24adbd1acf24492c97c10f73d75979fe |
| Source note | uspto-grants-2002_06 |