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HRID 1107768作成日:2026年10月26日

2-Chloro-6-fluorobenzyl alcohol → 1-(2-Butenyl)-7-(2-chloro-6-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1107768

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-6-fluorobenzyl alcoholHCID 91868—
反応物1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 53719624—
生成物1-(2-Butenyl)-7-(2-chloro-6-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 5371684957.6%

反応手順

The title compound (cis/trans=21/79) was prepared as a pale brown powder in 57.60% yield in a similar procedure to that described in Example 1 by using 1-(2-butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=24/76) and 2-chloro-6-fluorobenzyl alcohol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06063782
出典データセットuspto-grants-2000_05
ORD IDord-b399ab50b4964b8d832710991b0613ed
出典メモuspto-grants-2000_05