5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

Base Information

Chemical Name:5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one
CAS No.:120135-14-0
Molecular Formula:C₂₉H₄₁ClN₂OS
Molecular Weight:501.176
Hs Code.:

Synonyms:5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

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Chemical Property of 5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

Chemical Property:

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Technology Process of 5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

There total 7 articles about 5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-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:

: 183130-05-4
2-Amino-N-[3-(2-chloro-benzoyl)-5-hexadecyl-thiophen-2-yl]-acetamide

: 120135-14-0
5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

Guidance literature:: With acetic acid; In isopropyl alcohol; for 20h; Yield given; Heating;
DOI:10.1016/0223-5234(96)85877-6

Reference yield:

: 638-66-4
n-Octadecanal

: 120135-14-0
5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine, sulfur / dimethylformamide / 4 h / 50 - 60 °C

2: CHCl₃ / 2 h / Heating

3: sodium iodide / tetrahydrofuran / 2 h / Heating

4: liquid ammonia / tetrahydrofuran / 4 h / -30 - 20 °C

5: acetic acid / propan-2-ol / 20 h / Heating

With ammonia; sulfur; acetic acid; triethylamine; sodium iodide; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/0223-5234(96)85877-6

Reference yield:

: 40018-25-5
2-Chlorobenzoyl acetonitrile

: 120135-14-0
5-(2-chlorophenyl)-7-hexadecyl-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine, sulfur / dimethylformamide / 4 h / 50 - 60 °C

2: CHCl₃ / 2 h / Heating

3: sodium iodide / tetrahydrofuran / 2 h / Heating

4: liquid ammonia / tetrahydrofuran / 4 h / -30 - 20 °C

5: acetic acid / propan-2-ol / 20 h / Heating

With ammonia; sulfur; acetic acid; triethylamine; sodium iodide; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/0223-5234(96)85877-6