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HRID 432135作成日:2026年10月25日

Acetic Acid → HCID 22347030、化合物

https://huagongshe.com/reaction/432135

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1-(Isopropyl)-4-piperidoneHCID 79313—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-(4-phenoxyphenyl)-1-(piperidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 22347262—
溶媒1,2-DichloroethaneHCID 11—
溶媒WaterHCID 962—
生成物HCID 22347030HCID 2234703045.1%

反応手順

3-(4-phenoxyphenyl)-1-(4-piperidinyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (Compound 2) (221 mg, 0.572 mmol), 1-isopropyl-4-piperidone(89 mg, 0.63 mmol), sodium triacetoxyborohydride (182 mg, 0.86 mmol) and glacial acetic acid(40 ul, 0.63 mmol) were mixed with 3 ml of 1,2-dichloroethane. After stirring at room temperature overnight, 2 ml of water was added followed by solid sodium bicarbonate until PH reached about 8. The layers were separated and the aqueous layer was extracted with dichloromethane. The combined organic layer was washed, dried and evaporated. The residue was purified by flash column chromatography to give 132 mg of 1-[1-(1-isopropyl-4-piperidinyl)-4-piperidinyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine. 1H NMR (DMSO) 0.99 (d, J=6.54 Hz, 6H), 1.42 (m, 2H), 1.72(d, J=11.41 Hz, 2H), 1.88 (d, J=9.61 Hz, 2H), 2.14 (s, 3H), 2.16 (m, 6H), 2.66 (m, 2H), 2.83(d, J=10.98 Hz, 2H), 2.98(d, J=8.25 Hz, 2H), 4.62 (m, 1H), 7.16 (m, 5H), 7.44 (m, 2H), 7.67 (d, J=8.69 Hz, 2H), 8.23 (s, 1H); LC/MS (MH+=512).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660744B1
出典データセットuspto-grants-2003_12
ORD IDord-452352a6fc8f4534a0cf331e6976e8e1
出典メモuspto-grants-2003_12