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HRID 700作成日:2026年10月23日

5-Bromo-2-chloroanisole → Tert-butyl 2-(4-chloro-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydropyrrolo[3,4-c]pyrrole-5-carboxylate

https://huagongshe.com/ja/reaction/700

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-chloroanisoleHCID 2769567—
反応物Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
試薬Sodium t-butoxideHCID 23676156—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物Tert-butyl 2-(4-chloro-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydropyrrolo[3,4-c]pyrrole-5-carboxylateHCID 5981395364.57%

反応条件

温度90 °C

反応手順

A mixture of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (205 mg, 0.97 mmol), 5-Bromo-2-chloroanisole (235 mg, 1.06 mmol), Sodium tert- butoxide (130 mg, 1.35 mmol), rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (30.1 mg, 0.05 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (44.2 mg, 0.05 mmol) in toluene (10 mL) under a nitrogen atmosphere was stirred at 90 °C for 12h. The solution was washed with saturated NaHCO3 solution, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude material was loaded on a 24g silica gel column and purified on a Teledyne Isco instrument, eluting with 20% to 40% ethyl acetate in heptane to provide tert-butyl 5-(4-chloro-3-methoxyphenyl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (220 mg, 64.6 %) as a solid. Used directly for the next step. MS m/z 353.3 [M+H]+ (ESI)

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-b0d4d24d68264e0ba39e9d5692455d36
出典メモ750 AstraZeneca ELN dataset