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HRID 1963705作成日:2026年10月24日

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylate

https://huagongshe.com/ja/reaction/1963705

反応式

関与物質

役割名称HCID仕込み量
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
反応物[4-(2-Amino(4-pyridyloxy))-2-nitrophenyl]methylamineHCID 69006232—
溶媒DimethylformamideHCID 6228—
生成物tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylateHCID 69038249—

反応手順

To a mixture of 1-(tert-butoxy)carbonylpiperidine-4-carboxylic acid (1 eq) in N,N-dimethyl formamide and N,N-disopropylethylamine (4 eq) was added BOP (2 eq) and the mixture was stirred at ambient temperature until homogeneous. To it was added [4-(2-amino(4-pyridyloxy))-2-nitrophenyl]methylamine (1 eq) and the resulting mixture was stirred at 60° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and the resulting tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylate was purified by silica gel chromatography. MS: MH+=472.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415382B2
出典データセットuspto-grants-2013_04
ORD IDord-9d0fa942aa18481bb5415e11a6c1960f
出典メモuspto-grants-2013_04