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HRID 902469作成日:2026年10月25日

1-(Thien-2-ylcarbonyl)piperazine → 5-Oxo-7-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile

https://huagongshe.com/reaction/902469

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Thien-2-ylcarbonyl)piperazineHCID 797562—
反応物7-Chloro-5-oxo-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrileHCID 59702077—
生成物5-Oxo-7-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrileHCID 59702116—

反応手順

To yield a compound of structure (II) with R2 as carbonitrile, R3 as thiophene, and R1 as defined above, the intermediate 7-chloro-5-oxo-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile, depicted by formula (33), was reacted with piperazin-1-yl-thiophene-2-yl-methanone to yield 5-oxo-7-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile, depicted by formula (34), which was either reacted with an appropriate halide (R1—X) or boronic acid (R1—B(OH)2) to yield target compounds of structure (II) with R2 as carbonitrile, R3 as thiophene, and R1 as defined above, as shown in Scheme 16.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365200B2
出典データセットuspto-grants-2008_04
ORD IDord-8d94f9b940354829b11093ed20061b75
出典メモuspto-grants-2008_04