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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62458생성일: 2026년 10월 27일

Triethylamine → N-((3-chloropyrazin-2-yl)methyl)-3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxamide

https://huagongshe.com/reaction/62458

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DiphosgeneHCID 10426—
반응물DiisopropylethylamineHCID 81531—
반응물3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochlorideHCID 11961371—
반응물(3-Chloropyrazin-2-yl)methanamine hydrochlorideHCID 42614233—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N-((3-chloropyrazin-2-yl)methyl)-3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxamideHCID 8667465299%

반응 조건

온도0 °C

반응 단계

A stirred solution of trichloromethyl carbonochloridate (1.038 g, 5.25 mmol) in tetrahydrofuran (10 mL) was cooled to 0° C. and a solution of 3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride (1 g, 4.37 mmol, J. Med. Chem., 2005, 141) and N-ethyl-N-isopropylpropan-2-amine (1.131 g, 8.75 mmol) in tetrahydrofuran (10 mL) was added slowly in 25 minutes. After stirring at 0° C. for one hour the solids were removed by filtration and the filtrate was concentrated in vaccuo (50° C. bath temperature). The residue was added to a solution of (3-chloropyrazin-2-yl)methanamine hydrochloride (0.788 g, 4.37 mmol) and triethylamine (1.018 g, 10.06 mmol) in dichloromethane (20 mL) and the reaction mixture was stirred for three hours. The solids were removed by filtration and the filtrate was concentrated in vacuo. Purification using column chromatography (silica gel; gradient dichloromethane/methanol 100:0 to 95:5) to afford N-((3-chloropyrazin-2-yl)methyl)-3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxamide (1.56 g, 4.31 mmol, 99% yield). LC-MS: C12H11ClF3N7O: 361. found 362.04[M+H]+, RT=0.42 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446130B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-3c34b64f6ed44ffa95a8318344aab70b
출처 메모uspto-grants-2016_09