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C20H19N5O4

Base Information
  • Chemical Name:C20H19N5O4
  • CAS No.:1092803-54-7
  • Molecular Formula:C20H19N5O4
  • Molecular Weight:393.402
  • Hs Code.:
C<sub>20</sub>H<sub>19</sub>N<sub>5</sub>O<sub>4</sub>

Synonyms:C20H19N5O4

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Chemical Property of C20H19N5O4
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Technology Process of C20H19N5O4

There total 15 articles about C20H19N5O4 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:
Guidance literature:
C47H45N5O4Si; With 2,3-dicyano-5,6-dichloro-p-benzoquinone;
With triethylamine tris(hydrogen fluoride); triethylamine;
Guidance literature:
Multi-step reaction with 17 steps
1.1: sodium hydride / N,N-dimethyl-formamide / 1.17 h / Cooling with ice
2.1: water; acetic acid / 16 h / 20 °C
3.1: sodium periodate / 1,4-dioxane; water / 1.67 h
4.1: sodium hydroxide / water; tetrahydrofuran / 72 h / 20 °C / Cooling with ice
5.1: triethylamine / dichloromethane; methanol / 18 h / 0 - 20 °C
6.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.75 h / -78 °C
7.1: n-butyllithium / tetrahydrofuran / 2 h / 0 °C
7.2: 16.33 h / -78 - 20 °C
8.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 24 h / 20 °C
8.2: 4 h / 50 °C
9.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.75 h / -78 °C
9.2: 0.5 h
10.1: triphenylphosphine / dichloromethane / 0.5 h / 0 °C
10.2: 2 h / -78 °C
11.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone; water / dichloromethane / 6 h / 20 °C
12.1: tetrahydrofuran; hexanes / 0.5 h / -78 °C
13.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 4 h / 0 - 20 °C
14.1: acetic anhydride; sulfuric acid; acetic acid
14.2: Reflux
15.1: dmap
16.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride
17.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone
With dmap; sodium periodate; n-butyllithium; oxalyl dichloride; 2,2'-azobis(isobutyronitrile); sulfuric acid; water; tri-n-butyl-tin hydride; acetic anhydride; sodium hydride; acetic acid; dimethyl sulfoxide; triethylamine; 9-bora-bicyclo[3.3.1]nonane; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; hexanes; dichloromethane; water; N,N-dimethyl-formamide; mineral oil; 14.2: Vorbrugen Reaction;
Guidance literature:
Multi-step reaction with 16 steps
1.1: water; acetic acid / 16 h / 20 °C
2.1: sodium periodate / 1,4-dioxane; water / 1.67 h
3.1: sodium hydroxide / water; tetrahydrofuran / 72 h / 20 °C / Cooling with ice
4.1: triethylamine / dichloromethane; methanol / 18 h / 0 - 20 °C
5.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.75 h / -78 °C
6.1: n-butyllithium / tetrahydrofuran / 2 h / 0 °C
6.2: 16.33 h / -78 - 20 °C
7.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 24 h / 20 °C
7.2: 4 h / 50 °C
8.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.75 h / -78 °C
8.2: 0.5 h
9.1: triphenylphosphine / dichloromethane / 0.5 h / 0 °C
9.2: 2 h / -78 °C
10.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone; water / dichloromethane / 6 h / 20 °C
11.1: tetrahydrofuran; hexanes / 0.5 h / -78 °C
12.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 4 h / 0 - 20 °C
13.1: acetic anhydride; sulfuric acid; acetic acid
13.2: Reflux
14.1: dmap
15.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride
16.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone
With dmap; sodium periodate; n-butyllithium; oxalyl dichloride; 2,2'-azobis(isobutyronitrile); sulfuric acid; water; tri-n-butyl-tin hydride; acetic anhydride; sodium hydride; acetic acid; dimethyl sulfoxide; triethylamine; 9-bora-bicyclo[3.3.1]nonane; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; hexanes; dichloromethane; water; N,N-dimethyl-formamide; mineral oil; 13.2: Vorbrugen Reaction;
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