4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

Base Information

Chemical Name:4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one
CAS No.:892113-72-3
Molecular Formula:C₁₇H₁₇F₆N₃O₂
Molecular Weight:409.331
Hs Code.:

Synonyms:4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

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Chemical Property of 4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

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Technology Process of 4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

There total 3 articles about 4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-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:

: 892113-66-5
4-[3-oxo-4-(2,4,5-trifluorophenyl)butanoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

: 892113-72-3
4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

Guidance literature:: 4-[3-oxo-4-(2,4,5-trifluorophenyl)butanoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one; With ammonium acetate; In isopropyl alcohol; at 45 ℃; for 3h;

In water; isopropyl alcohol; at 30 ℃; for 0.25h;

Reference yield:

: 2-[(2-cyanoethyl)amino]-4,4,4-trifluorobutanoic acid

: 892113-72-3
4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen; sodium methylate / Raney nickel-2800 / methanol; water / 18 h / 25 °C / 5414.51 Torr

2.1: hydrogenchloride / methanol / 20 - 33 °C

2.2: 20 - 26 °C

2.3: 20 - 29 °C / pH 3

3.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 12 h / 40 °C

4.1: ammonium acetate / tert-butyl methyl ether; isopropyl alcohol / 3 h / 45 °C

4.2: 0.25 h / 20 - 30 °C

With hydrogenchloride; ammonium acetate; hydrogen; sodium methylate; N-ethyl-N,N-diisopropylamine; Raney nickel-2800; In methanol; tert-butyl methyl ether; water; isopropyl alcohol; acetonitrile;

Reference yield:

: 209995-38-0
(2,4,5-trifluorophenyl)acetic acid

: 892113-72-3
4-[(2Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: dmap; pivaloyl chloride; N-ethyl-N,N-diisopropylamine / acetonitrile / 3 - 5 h / 20 - 55 °C

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 12 h / 40 °C

3.1: ammonium acetate / tert-butyl methyl ether; isopropyl alcohol / 3 h / 45 °C

3.2: 0.25 h / 20 - 30 °C

With dmap; ammonium acetate; pivaloyl chloride; N-ethyl-N,N-diisopropylamine; In tert-butyl methyl ether; isopropyl alcohol; acetonitrile;