5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

Base Information

Chemical Name:5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one
CAS No.:40018-15-3
Molecular Formula:C₁₄H₉F₃N₂OS
Molecular Weight:310.299
Hs Code.:

5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-<i>e</i>][1,4]diazepin-2-one

Synonyms:5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

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Chemical Property of 5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

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Technology Process of 5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

There total 9 articles about 5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 52.0%

: 40018-14-2
2-Amino-N-[3-(2-trifluoromethyl-benzoyl)-thiophen-2-yl]-acetamide

: 40018-15-3
5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

Guidance literature:: With Trimethylacetic acid; for 0.5h; Heating;
DOI:10.1002/ardp.19803130704

Reference yield:

: 447-60-9
2-(trifluoromethyl)benzonitrile

: 40018-15-3
5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

Guidance literature:: Multi-step reaction with 7 steps

1: 29 percent / Na / benzene / Heating; 1.) 4 h, reflux, 2.) 12 h, room temp.

2: 88 percent / conc. aq. HCl

3: 78 percent / Et₃N / dioxane / 0.5 h / Heating

4: K₂CO₃ / dioxane / 2 h / Ambient temperature

5: NaI / acetone / 1 h / Heating

6: 86 percent / conc. aq. NH₃ / CH₂Cl₂ / 48 h / Ambient temperature

7: Heating

With hydrogenchloride; ammonium hydroxide; sodium; potassium carbonate; triethylamine; sodium iodide; In 1,4-dioxane; dichloromethane; acetone; benzene;
DOI:10.1002/ardp.19803130704

Reference yield:

: 40018-09-5
o-Trifluormethylbenzoacetodinitril

: 40018-15-3
5-(2-trifluoromethyl-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: 88 percent / conc. aq. HCl

2: 78 percent / Et₃N / dioxane / 0.5 h / Heating

3: K₂CO₃ / dioxane / 2 h / Ambient temperature

4: NaI / acetone / 1 h / Heating

5: 86 percent / conc. aq. NH₃ / CH₂Cl₂ / 48 h / Ambient temperature

6: Heating

With hydrogenchloride; ammonium hydroxide; potassium carbonate; triethylamine; sodium iodide; In 1,4-dioxane; dichloromethane; acetone;
DOI:10.1002/ardp.19803130704