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HRID 30783作成日:2026年10月23日

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → ((1-Ethyl)(4-piperidyl))-n-{4-{4-(methylamino)-3-nitrophenoxy}(2-pyridyl)}carboxamide

https://huagongshe.com/ja/reaction/30783

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-Ethylpiperidine-4-carboxylic acidHCID 18783773—
反応物[4-(2-Amino(4-pyridyloxy))-2-nitrophenyl]methylamineHCID 69006232—
溶媒DimethylformamideHCID 6228—
生成物((1-Ethyl)(4-piperidyl))-n-{4-{4-(methylamino)-3-nitrophenoxy}(2-pyridyl)}carboxamideHCID 131727053—

反応手順

To a mixture of 1-(ethyl)piperidine-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 ((1-ethyl)(4-piperidyl))-N-{4-[4-(methylamino)-3-nitrophenoxy]}(2-pyridyl))carboxamide was purified by silica gel chromatography. MS: MH+=400.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423150B2
出典データセットuspto-grants-2008_09
ORD IDord-c934a1c0009446a6869700f9a3caa1a6
出典メモuspto-grants-2008_09