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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536638생성일: 2026년 10월 25일

N-cyclohexyl-N'-(2-morpholinoethyl)-carbodiimide methyl-p-toluenesulfonate → 4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-one

https://huagongshe.com/reaction/536638

반응식

참여 물질

역할이름HCID투입량
반응물N-cyclohexyl-N'-(2-morpholinoethyl)-carbodiimide methyl-p-toluenesulfonateHCID 9954069—
반응물3-Carboxymethyl-5-methoxy-indan-1-yl-ammonium chlorideHCID 86656208—
용매PyridineHCID 1049—
생성물4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-oneHCID 66941775—

반응 단계

3-Carboxymethyl-5-methoxy-indan-1-yl-ammonium chloride (13.2 g) and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate (21.7 g) dissolved in pyridine (500 mL) is stirred at room temperature for 7 d. Then, the pyridine is removed under reduced pressure and the residue is taken up in water (200 mL) and dichloromethane (200 mL). The organic phase is separated and the aqueous phase is extracted twice with dichloromethane. The combined organic phases are washed with 1 M hydrochloric acid, 1 M NaOH solution, and water. After drying (MgSO4), the solvent is evaporated under reduced pressure to yield the product as a beige solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859580B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-be2ab3346de140baa63765b2ac1f6b83
출처 메모uspto-grants-2014_10