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HRID 2201126作成日:2026年10月25日

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → (R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-(thiophen-2-yl)propanamide

https://huagongshe.com/reaction/2201126

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
反応物3-Methylisothiazol-5-ylamine hydrochlorideHCID 2723918—
反応物Sodium Phenoxide TrihydrateHCID 23681143—
反応物(R)-2-(3-bromo-4-cyanophenylamino)-3-(thiophen-2-yl)propanamideHCID 67508155—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物(R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-(thiophen-2-yl)propanamideHCID 6750879733.9%

反応手順

A mixture of (R)-2-(3-bromo-4-cyanophenylamino)-3-(thiophen-2-yl)propanamide (35 mg, 0.100 mmol), 5-amino-3-methylisothiazole hydrochloride (25 mg, 0.166 mmol), sodium phenoxide trihydrate (52 mg, 0.305 mmol), xantphos (14 mg, 0.024 mmol) and Pd2 dba3 (10 mg, 0.010 mmol) in dioxane (2 mL) was degassed with argon, then was heated by microwave at 170 C for 30 min. The mixture was concentrated in vacuo. The residue was purified by HPLC to give (R)-2-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-(thiophen-2-yl)propanamide (13 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359375B2
出典データセットuspto-grants-2016_06
ORD IDord-06fbf081666d425e8da0bae9566d859b
出典メモuspto-grants-2016_06