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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542010생성일: 2026년 10월 25일

2-(Isocyanatomethyl)furan → 4-(2-{[6-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]oxy}ethyl)-N-(2-furylmethyl)piperidine-1-carboxamide bis(trifluoroacetate)

https://huagongshe.com/reaction/542010

반응식

참여 물질

역할이름HCID투입량
반응물2-(Isocyanatomethyl)furanHCID 4223811—
반응물6-Chloro-12-(2-piperidin-4-ylethoxy)-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene tris(trifluoroacetate)HCID 86636347—
생성물4-(2-{[6-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]oxy}ethyl)-N-(2-furylmethyl)piperidine-1-carboxamide bis(trifluoroacetate)HCID 8663635040%

반응 단계

The desired compound was prepared according to the procedure of Example D41 using 6-chloro-12-(2-piperidin-4-ylethoxy)-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene tris(trifluoroacetate) and 2-(isocyanatomethyl)furan as the starting materials in 40% yield. LCMS for C30H33ClN7O3 (M+H)+: m/z=574.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871753B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-62cfb5ffc55942c08b49a5cbc97491c7
출처 메모uspto-grants-2014_10