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HRID 40508作成日:2026年10月25日

2-(Di-tert-butylphosphino)biphenyl → (1-{4-[3-(4-Cyclopropylmethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/40508

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Di-tert-butylphosphino)biphenylHCID 2734215—
反応物Sodium t-butoxideHCID 23676156—
反応物(S)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamateHCID 56973617—
反応物3-(4-Cyclopropylmethoxy-phenoxy)-azetidineHCID 86689009—
溶媒1,4-DioxaneHCID 31275—
生成物(1-{4-[3-(4-Cyclopropylmethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-carbamic acid tert-butyl esterHCID 86689011—

反応条件

温度45 °C

反応手順

To 0.9 g (4.1 mmol) 3-(4-cyclopropylmethoxy-phenoxy)-azetidine (IX.1), 1.2 g (4.1 mmol) (S)-[1-(4-bromo-phenyl)-ethyl]-carbamic acid tert-butyl ester (I.3), 1.6 g (16.4 mmol) NaOtBu, 0.49 g (1.64 mmol) 2-(di-tert-butylphosphino)biphenyl and 0.38 g (0.41 mmol) tris-(dibenzylideneacetone)-dipalladium(0) are added under an argon atmosphere 25 mL 1,4-dioxane. The mixture is stirred for 12 h at 45° C. The mixture is filtered, washed with MeOH and concentrated. The residue is purified by HPLC (silica gel; PE/ethyl acetate; gradient 9:1→1:1) to yield the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530461B2
出典データセットuspto-grants-2013_09
ORD IDord-43dd1fb6b8df4c818bac9889d4be644f
出典メモuspto-grants-2013_09