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HRID 38566作成日:2026年10月24日

3-Chloro-4-(3-fluorobenzyloxy)aniline → tert-Butyl 4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-5,8-dihydropyrido[4',3':4,5]furo-[2,3-d]pyrimidine-7(6H)-carboxylate

https://huagongshe.com/ja/reaction/38566

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 7059263—
反応物tert-Butyl 3-cyano-2-[(1-methoxymethylidene)amino]-4,7-dihydrofuro[2,3-c]pyridine-6(5H)-carboxylateHCID 70796469—
溶媒MethanolHCID 887—
生成物tert-Butyl 4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-5,8-dihydropyrido[4',3':4,5]furo-[2,3-d]pyrimidine-7(6H)-carboxylateHCID 70915423—

反応手順

tert-Butyl 3-cyano-2-[(1-methoxymethylidene)amino]-4,7-dihydrofuro[2,3-c]pyridine-6(5H)-carboxylate from Example 47A (134 mg, 0.44 mmol) and 3-chloro-4-[(3-fluorobenzyl)oxy]aniline from Example 4A (221 mg, 0.88 mmol) were heated in methanol (3.0 mL) in a microwave oven for 1 h at 160° C. The title compound was isolated by preparative HPLC to yield 18 mg (8%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524722B2
出典データセットuspto-grants-2013_09
ORD IDord-7c2627be5ce54f51902e18c10e243ad2
出典メモuspto-grants-2013_09