反应 #1845851
相关文献 (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US07576122B2
反应条件: temp:45.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 29 mg [2-(2,2-dimethylpropanoyl)-5-methoxy-1-benzofuran-3-yl]acetic acid from the Step B Example 1, 23 mg HOBt, and 38.3 mg EDC was added 1 mL dry DMF. Add 24.9 mg (3,3-dimethylbutyl)amine hydrochloride followed by 61 μL DIEA. This solution was heated at 45° C. for 2 hours. It was purified directly on RP-HPLC using 60-75% MeCN gradient. The fractions containing pure product were pooled and lyophilized to give the title compound. LC-MS: 4.08 min. (m/Z=290.1, 374.2, 396.2). It was purified directly on RP-HPLC using 60-75% MeCN gradient The fractions containing pure product
来源 ID: ord-6552561b9ccc42928a1e4f6d50ed9a22