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HRID 62449作成日:2026年10月24日

Triphenylphosphine → HCID 90303937、化合物

https://huagongshe.com/ja/reaction/62449

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物1-tosyl-4,5,6,7-tetrahydro-1H-indazol-4-olHCID 90304168—
反応物HCID 178491029HCID 178491029—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 90303937HCID 9030393732.4%

反応手順

A solution of 1-tosyl-4,5,6,7-tetrahydro-1H-indazol-4-ol (4.05 g, 11.13 mmol), 3-bromo-N-(2,4-dimethoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (3.9 g, 13.35 mmol) and PPh3 (4.38 g, 16.70 mmol) in dry THF (110 mL) at 0° C. was added dropwise DIAD (3.37 g, 16.70 mmol) over a period of 5 minutes under a nitrogen atmosphere, then the mixture was stirred at room temperature for 4 hours. Removed the solvent under reduced pressure and then extracted with DCM, the combined organic layer was washed with water, brine and dried over anhydrous Na2SO4. The organic layer was concentrated in vacuo and the residue was purified by preparative HPLC separation to afford 3-bromo-N-(2,4-dimethoxybenzyl)-1-(1-tosyl-4,5,6,7-tetrahydro-1H-indazol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2.3 g, yield 32.4%). MS-ESI (m/z): 640 (M+2)+ (Acq Method: 10-80AB_2 min; Rt: 1.357 min)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446130B2
出典データセットuspto-grants-2016_09
ORD IDord-5ca6649f5c814447b4fbfc149626ab43
出典メモuspto-grants-2016_09