With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.104291-83-0,Methyl 6-cyano-1H-indole-2-carboxylate,as a common compound, the synthetic route is as follows.
Methyl 6-cyano-1H-indole-2-carboxylate (467 mg, 2.33 mmol) was dissolved in N,N-dimethylformamide (25 mL) and cooled in an ice bath. NaH (60%, 112 mg, 2.80 mmol) was added and the reaction mixture was stirred for 10 min. 2-(Chloromethyl)-1,3,5-trimethyl-benzene (472 mg, 2.80 mmol) was added and the reaction mixture was allowed to warm to room temperature and was stirred for 12 h. The reaction mixture was poured into ice water and was made acidic with the addition of 1 N HCl. The resulting precipitate was collected to give methyl 6-cyano-1-(2,4,6-trimethylbenzyl)-1H-indole-2-carboxylate. ESI-MS m/z calc. 332.2. found 333.2 (M+1)+. Retention time: 0.81 min (1 min run)., 104291-83-0
The synthetic route of 104291-83-0 has been constantly updated, and we look forward to future research findings.
Reference:
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