Simple exploration of 864274-04-4

As the paragraph descriping shows that 864274-04-4 is playing an increasingly important role.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.864274-04-4,2-Methylbenzo[d]oxazole-6-carbaldehyde,as a common compound, the synthetic route is as follows.

864274-04-4, Example 61; 2-(2-Fluoro-phenylimino)-5-(2-methyl-benzooxazol-6-yl-methvlene)-thiazolidin-4-one; To the solution of 2-(2, 6-difluoro-phenylimino)-thiazolidin-4-one (105 mg, 0.5 mmol) in ethanol (5 mL) was added 2-methyl-benzooxazole-6-carbaldehyde (80 mg, 0. 5 mmol, 1 eq) followed by piperidine (0.1 mL). The reaction mixture was refluxed for 48 hours and diethyl ether (3 mL) was added. Solid was filtered to give 58 mg (33 percent yield) of pure 2-(2-fluoro-phenylimino)-5-(2-methyl-benzooxazol-6-yl-methylene)-thiazolidin-4-one. LC MS (m/e) = 354.2 (MH+). Rt = 2.11 min.

As the paragraph descriping shows that 864274-04-4 is playing an increasingly important role.

Reference£º
Patent; SMITHKLINE BEECHAM CORPORATION; WO2005/82901; (2005); A1;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem