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HRID 57631作成日:2026年10月26日

Triethylamine → (S)-tert-butyl 2-((7-(4-(4-(cyclopropylsulfonyl)piperazin-1-yl)phenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/57631

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Cyclopropanesulfonyl chlorideHCID 2760919—
反応物(S)-tert-butyl 2-((7-(4-(piperazin-1-yl)phenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylateHCID 86717391—
溶媒DichloromethaneHCID 6344—
生成物(S)-tert-butyl 2-((7-(4-(4-(cyclopropylsulfonyl)piperazin-1-yl)phenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylateHCID 8671739342.6%

反応手順

A solution of (S)-tert-butyl 2-((7-(4-(piperazin-1-yl)phenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylate (100 mg, 0.20 mmol), cyclopropanesulfonyl chloride (33 mg, 0.24 mmol) and Et3N (41 mg, 0.40 mmol) in 5 mL of DCM at 0° C. was stirred at room temperature for 1 hour. The volatiles were removed in vacuo, and the residues was purified by chromatography with PE/EA (1:2˜1:10) to give 52 mg of title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434726B2
出典データセットuspto-grants-2016_09
ORD IDord-7a707564977b42a09ab523be24f057d4
出典メモuspto-grants-2016_09