TH385B - 5- phenyl ethenyl benzimidazole - Google Patents
5- phenyl ethenyl benzimidazoleInfo
- Publication number
- TH385B TH385B TH8301000518A TH8301000518A TH385B TH 385 B TH385 B TH 385B TH 8301000518 A TH8301000518 A TH 8301000518A TH 8301000518 A TH8301000518 A TH 8301000518A TH 385 B TH385 B TH 385B
- Authority
- TH
- Thailand
- Prior art keywords
- small
- hydrogen
- methyl
- react
- alkyl
- Prior art date
Links
- GJQKKMMGXMDMSS-UHFFFAOYSA-N C=CC1=NC(C=CC(C2=CC=CC=C2)=C2)=C2N1 Chemical compound C=CC1=NC(C=CC(C2=CC=CC=C2)=C2)=C2N1 GJQKKMMGXMDMSS-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims 1
- 101100343714 Mus musculus Loxl4 gene Proteins 0.000 claims 1
- NLALZHBMLLVTHQ-UHFFFAOYSA-N OBr=O.N#CC#N Chemical compound OBr=O.N#CC#N NLALZHBMLLVTHQ-UHFFFAOYSA-N 0.000 claims 1
- 229930013930 alkaloid Natural products 0.000 claims 1
- 150000003797 alkaloid derivatives Chemical class 0.000 claims 1
- -1 alkyl chloroformate Chemical compound 0.000 claims 1
- 150000001350 alkyl halides Chemical class 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 claims 1
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 claims 1
- ZOOSILUVXHVRJE-UHFFFAOYSA-N cyclopropanecarbonyl chloride Chemical compound ClC(=O)C1CC1 ZOOSILUVXHVRJE-UHFFFAOYSA-N 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 claims 1
- MMBDAJMDNVQFDV-UHFFFAOYSA-N methyl n-[amino(methylsulfanyl)methylidene]carbamate Chemical compound COC(=O)N=C(N)SC MMBDAJMDNVQFDV-UHFFFAOYSA-N 0.000 claims 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract 1
- 244000045947 parasite Species 0.000 abstract 1
Abstract
ได้เตรียม 2-แอซิลอะมิโน-5-เฟนิลเอเธนิลเบนซิมิดาโซลต่าง ๆชนิดใหม่ แลได้พบว่ามีฤทธิ์ทำลายพยาธิได้ สารประกอบชนิดหนึ่งของการประดิษฐ์นี้ คือ เมธิล [5-(1-เฟนิลเอเธนิล)-1H-เปบนซิมิดาโซล-2-อิล]คาร์บาเมท Various new types of 2-acylamino-5-phenylethenylbenzimidazole were prepared and it was found to be effective against parasites. One of the compounds of this invention is methyl[5-(1-phenylethhenyl)-1H-pebonsimidazole-2-il]carbamate.
Claims (5)
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH1547A TH1547A (en) | 1984-05-01 |
| TH385B true TH385B (en) | 1986-05-02 |
Family
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