돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2109176생성일: 2026년 10월 25일

Sodium Hydroxide → 3-[4-(6-amino-pyridin-3-yl)-[1,2,3]triazol-1-yl]-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-4-methyl-benzamide

https://huagongshe.com/reaction/2109176

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물3-azido-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-4-methyl-benzamideHCID 21079202—
반응물4-Ethynylpyridin-2-amineHCID 21097262—
반응물Sodium AscorbateHCID 23667548—
촉매Copper SulfateHCID 24462—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물3-[4-(6-amino-pyridin-3-yl)-[1,2,3]triazol-1-yl]-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-4-methyl-benzamideHCID 2109709581%

반응 단계

To a stirring suspension of 310 mg (0.719 mmol) of 3-azido-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-4-methyl-benzamide in 2 mL of EtOH and 2 mL of water was added dropwise 4M NaOH until the mixture became homogeneous. A solution of 142 mg (0.719 mmol) of sodium ascorbate in 0.5 mL of water was added, followed by 100 mg (0.719 mmol) 2-amino-4-ethynyl pyridine in 1 mL of EtOH. Finally 0.72 mL of 0.1 M CuSO4 was added, and the resulting mixture was stirred vigorously for 14 h. The mixture was then diluted with 40 mL of water and HOAc was added until a precipitate formed and the pH was about 6. The precipitate was filtered and washed with water and hexanes. The solids were chromatographed (0-5% MeOH/0.5% NH4OH in CH2Cl2) to provide 321 mg (0.584 mmol; 81% of the title compound. ESI MS m/z 548 [C27H31N7O4S—H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07514458B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-7d73089d60114631bd18c5dd6e157d95
출처 메모uspto-grants-2009_04