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HRID 587143作成日:2026年10月26日

tert-butyl N-((piperidin-2-yl)methyl)carbamate → Tert-butyl [(1-(4-((3-(sulfamoylmethyl)phenyl)amino)-1,3,5-triazin-2-yl)piperidine-2-yl)methyl]carbamate

https://huagongshe.com/reaction/587143

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-((piperidin-2-yl)methyl)carbamateHCID 2756031—
反応物rac-3-[(4-(2-Methoxymethylpiperidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamideHCID 60197106—
反応物3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—
生成物Tert-butyl [(1-(4-((3-(sulfamoylmethyl)phenyl)amino)-1,3,5-triazin-2-yl)piperidine-2-yl)methyl]carbamateHCID 60197197—

反応手順

B7 was prepared following the procedure reported for B4 using A1 and rac-tert-butyl (piperidin-2-yl)methylcarbamate and obtained as a white crystalline solid; yield: 280 mg (65%). MS (ES) C21H31N7O4S requires: 477. found: 478 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09226929B2
出典データセットuspto-grants-2016_01
ORD IDord-f379f6e7cd824fd297cc9dee8346742e
出典メモuspto-grants-2016_01