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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14411생성일: 2026년 10월 23일

Benzaldehyde → 9-Amino-19-benzyl-14,32-dichloro-5-methyl-26-oxa-4-thia-3,8,10,16,19-pentaazatetracyclo[25.2.2.212,15.02,6] tritriaconta-1(29),2,5,8,12,14,23,27,30,32-decaene-7,17-dione

https://huagongshe.com/ko/reaction/14411

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참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Trimethyl orthoformateHCID 9005—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물9-Amino-14,32-dichloro-5-methyl-26-oxa-4-thia-3,8,10,16,19-pentaazatetracyclo[25.2.2.212,15.02,6]tritriaconta-1(29),2,5,8,12,14,23,27,30,32-decaene-7,17-dioneHCID 178435148—
용매Acetic AcidHCID 176—
생성물9-Amino-19-benzyl-14,32-dichloro-5-methyl-26-oxa-4-thia-3,8,10,16,19-pentaazatetracyclo[25.2.2.212,15.02,6] tritriaconta-1(29),2,5,8,12,14,23,27,30,32-decaene-7,17-dioneHCID 178435147—

반응 단계

The cis/trans mixture of the title compound of 9-amino-14,32-dichloro-5-methyl-26-oxa-4-thia-3,8,10,16,19-pentaazatetracyclo[25.2.2.212,15.02,6]tritriaconta-1(29),2,5,8,12,14,23,27,30,32-decaene-7,17-dione (Example 4) (60 mg), benzaldehyde (24 mg), sodium triacetoxyborohydride (30 mg), trimethyl orthoformate (0.2 mL) and acetic acid (0.1 mL), in 2 mL of DMF was stirred at room temperature for 16 hrs. Ethyl acetate (10 mL) and saturated sodium bicarbonate solution (10 mL) were added. Layers were separated after the mixture was well shaken. The organic layer was dried over anhydrous magnesium sulfate and solvent was evaporated in vacuo to give a crude product, which was purified by preparative HPLC to give 27 mg of the title compound as an inseparable mixture of cis/trans isomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732434B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8585272f986b43429b57b80fb10e19a7
출처 메모uspto-grants-2010_06