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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 636314생성일: 2026년 10월 26일

4-Methylmorpholine → 6-(1-Pyrenebutyryl)-3,10-bis(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1(16),12,14-triene

https://huagongshe.com/reaction/636314

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-Pyrenebutanoic acidHCID 76977—
반응물HCID 10555399HCID 10555399—
용매DichloromethaneHCID 6344—
생성물6-(1-Pyrenebutyryl)-3,10-bis(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1(16),12,14-trieneHCID 1072428092%

반응 단계

A mixture of 1-pyrenebutyric acid (0.87 g, 3.0 mmol) and 4-methylmorpholine (0.59 g, 5.9 mmol) in 20 mL of anhydrous CH2Cl2 was stirred at rt for 30 min. After addition of 1,3-dicyclohexylcarbodiimide (DCC) (0.62 g, 3.0 mmol) and 1-hydroxybenzotriazole (HOBT) (0.41 g, 3.0 mmol), the resulting solution was stirred at rt for another 30 min. A solution of 3,10-bis(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1(16),12,14-triene (from Example 72, 1.77 g, 3.0 mmol) was added to the above solution and the resulting solution was stirred at rt for 40 h. The solution was filtered and the filtrate was washed with brine , dried (Na2SO4) and concentrated. The residue was purified by flash chromatography on a silica gel column using 100:1 CH2Cl2—MeOH as an eluent to give 2.36 g (92%) of the title compound as a pale yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06191273B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-687c2ab313534964ac1e145c8309a1e3
출처 메모uspto-grants-2001_02