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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 633509생성일: 2026년 10월 26일

Ethanol → 6-[(6-Ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amine

https://huagongshe.com/reaction/633509

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물1,4-Dimercapto-2,3-butanediolHCID 19001—
반응물2-Amino-6-thiocyanato-1,3-benzothiazoleHCID 81600—
반응물HCID 67524522HCID 67524522—
촉매Monobasic potassium phosphateHCID 516951—
용매WaterHCID 962—
생성물6-[(6-Ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amineHCID 4259889580.3%

반응 단계

The 6-[(6-ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amine was prepared according to the method described in Example 17a, but using 587 mg of 2-amino-1,3-benzothiazol-6-yl thiocyanate (commercial), 20 cm3 of degassed ethanol, 13 mg of potassium dihydrogen phosphate in 0.2 cm3 of water, 1.31 g of DL-dithiothreitol and 562 mg of 3-chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine. 783 mg of 6-[(6-ethoxy[1,2,4]triazolo[4,3-b]pyridazin-3-yl)sulphanyl]-1,3-benzothiazol-2-amine are thus obtained in the form of a whitish powder, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321777B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-542b229f19334344b5bc98c618b6372f
출처 메모uspto-grants-2016_04