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HRID 230183作成日:2026年10月26日

Triethylamine → (R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol

https://huagongshe.com/reaction/230183

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物(S)-(+)-1-Aminopropan-2-olHCID 7311736—
反応物4-Chloro-6-methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidineHCID 86600485—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-olHCID 68876938107.4%

反応手順

4-Chloro-6-methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidine (391 mg, 1.182 mmol) was dissolved in 5 mL of dry THF. Triethylamine (239 mg, 2.363 mmol) was added, and the reaction mixture was stirred for four hours. (S)-1-Amino-propan-2-ol (93 mg, 1.241 mmol) was then added, and the reaction mixture was stirred for 64 hours. The reaction mixture was quenched by addition to water, and was partitioned between water and ethyl acetate. The organic layer was separated, dried over MgSO4, filtered, and evaporated under reduced pressure to give (R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol (469 mg). Mass Spec. M+H=370.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566708B2
出典データセットuspto-grants-2009_07
ORD IDord-d86f1e23ab0341ae9b8e4a580b21a1cb
出典メモuspto-grants-2009_07