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HRID 1469368作成日:2026年10月27日

2-[3-(2-Benzyloxy-ethoxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane → 3-{5-[3-(2-Benzyloxy-ethoxy)-phenyl]pyridin-2-yloxy}-azetidine-1-carboxylic acid pyridazin-3-ylamide

https://huagongshe.com/reaction/1469368

反応式

関与物質

役割名称HCID仕込み量
反応物2-[3-(2-Benzyloxy-ethoxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolaneHCID 58073128—
反応物US10918640, Example 14HCID 66710496—
生成物3-{5-[3-(2-Benzyloxy-ethoxy)-phenyl]pyridin-2-yloxy}-azetidine-1-carboxylic acid pyridazin-3-ylamideHCID 4421889928%

反応手順

This compound was prepared by the method outlined for example 5 step 6. Thus 3-(5-iodo-pyridin-2-yloxy)-azetidine-1-carboxylic acid pyridazin-3-ylamide (example 7, step 1) (600 mg, 1.15 mmol) was reacted with 2-[3-(2-benzyloxy-ethoxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (1.5 equiv). Crude product purified by flash chromatography on silica gel eluting with 4:1 ethyl acetate:hexane to afford title compound (214 mg, 28%) as a brown foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09006269B2
出典データセットuspto-grants-2015_04
ORD IDord-2a1ba5558fc04308a8d5c86791ef02c9
出典メモuspto-grants-2015_04