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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2409656생성일: 2026년 10월 24일

O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate → 8-(4-Methyl-thiophen-3-yl)-quinoxaline-5-carboxylic acid [5-(4-methyl-piperazin-1-ylmethyl)-pyridin-2-yl]-amide

https://huagongshe.com/ko/reaction/2409656

반응식

참여 물질

역할이름HCID투입량
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물4-Methyl-3-thiopheneboronic acidHCID 5083931—
반응물8-(4-Methylthiophen-3-yl)-quinoxaline-5-carboxylic acidHCID 66914550—
반응물HCID 66914562HCID 66914562—
용매Dichloromethane methanolHCID 21226129—
생성물8-(4-Methyl-thiophen-3-yl)-quinoxaline-5-carboxylic acid [5-(4-methyl-piperazin-1-ylmethyl)-pyridin-2-yl]-amideHCID 44516282—

반응 단계

The title compound was prepared in analogy to the procedure described in Step 14.1 but stirring the reaction mixture at rt overnight, using 2 equiv of 5-(4-methyl-piperazin-1-ylmethyl)-pyridin-2-ylamine hydrochloride (Example 31), TBTU (2 equiv) and 8-(4-methyl-thiophen-3-yl)-quinoxaline-5-carboxylic acid. The carboxylic acid was synthesized as described in Steps 1.2-1.7 but using 4-methyl-3-thiopheneboronic acid in Step 1.4. Title compound: ESI-MS: 459.1 [M+H]+; tR=3.41 min (System 1); TLC: Rf=0.25 (DCM/MeOH, 9:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08815901B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-dc1888f40dd140e48b4c85957aefdf9b
출처 메모uspto-grants-2014_08