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HRID 1476생성일: 2026년 10월 23일

Triethylamine → Isopropyl 3(2-chloro-4-fluoro-5-isothiocyanatophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate

https://huagongshe.com/ko/reaction/1476

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ThiophosgeneHCID 10040—
반응물isopropyl 3-(5-amino-2-chloro-4-fluorophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetateHCID 57313385—
용매TetrahydrofuranHCID 8028—
생성물Isopropyl 3(2-chloro-4-fluoro-5-isothiocyanatophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetateHCID 11729649—

반응 단계

Thiophosgene (0.50 mL, 6.5 mmol) is added over 45 minutes to a solution of isopropyl 3-(5-amino-2-chloro-4-fluorophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate (2.5 g, 6.5 mmol), and triethylamine (1.8 mL, 13.0 mmol) in tetrahydrofuran. The reaction mixture is stirred at room temperature for 4 hours, diluted with tetrahydrofuran, and filtered. The filtrate is concentrated in vacuo to give the title product as an orange oil which is identified by NMR spectral analyses, Using essentially the same procedure, but using the appropriately substituted 3-(5-amino-2-chloro-4-fluorophenyl)tetrahydro-2,4,6-trioxo-s-triazine, the following compounds are obtained:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726126
출처 데이터셋uspto-grants-1998_03
ORD IDord-abde48b4f1894595a808afe5690eeb6d
출처 메모uspto-grants-1998_03