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HRID 12959作成日:2026年10月24日

4-Cyanophenylboronic acid → (3aR,6aR)-5-methyl-1-(4'-pyrimidin-5-yl-1,1'-biphenyl-4-yl)octahydropyrrolo[3,4-b]pyrrole

https://huagongshe.com/ja/reaction/12959

反応式

関与物質

役割名称HCID仕込み量
反応物4-Cyanophenylboronic acidHCID 2734326—
反応物(Pyrimidin-5-yl)boronic acidHCID 2795193—
反応物(3aR,6aR)-1-(4-Bromophenyl)-5-methyloctahydropyrrolo[3,4-b]pyrroleHCID 44221503—
生成物(3aR,6aR)-5-methyl-1-(4'-pyrimidin-5-yl-1,1'-biphenyl-4-yl)octahydropyrrolo[3,4-b]pyrroleHCID 24743650—

反応手順

The title compound was prepared according to the procedure described in Example 7D, substituting the product of Example 41A for the product of Example 7C and substituting pyrimidine-5-boronic acid for 4-cyanophenylboronic acid. 1H NMR (300 MHz, CDCl3) δ ppm 9.19 (s, 1H) 8.99 (s, 2H) 7.62-7.74 (m, 4H) 7.52-7.58 (m, 2H) 6.63-6.70 (m, 2H) 4.20-4.31 (m, 1H) 3.55-3.67 (m, 1H) 3.30-3.42 (m, 1H) 2.99-3.14 (m, 1H) 2.60-2.84 (m, 4H) 2.42 (s, 3H) 2.16-2.26 (m, 1H) 1.95-2.05 (m, 1H); MS (M+H)+=357.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728031B2
出典データセットuspto-grants-2010_06
ORD IDord-77cd97a9d29b4edcae9d41b13b024132
出典メモuspto-grants-2010_06