N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

Base Information

Chemical Name:N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide
CAS No.:1093256-33-7
Molecular Formula:C₂₅H₁₆Cl₂FN₃O₃S
Molecular Weight:528.391
Hs Code.:

Synonyms:N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

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Chemical Property of N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

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Technology Process of N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

There total 15 articles about N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide 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: 38.0%

: 1093254-29-5
3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile

: 1093263-00-3
2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxylic acid

: 1093256-33-7
N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 37033-95-7
5-benzyloxy-1H-indole-2-carboxylic acid ethyl ester

: 1093256-33-7
N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1: PS-DMAP / tetrahydrofuran / 20 °C

2: ammonium formate / palladium on activated charcoal

3: triphenylphosphine / dichloromethane / 1 h / 45 °C

4: hydrogenchloride / tetrahydrofuran; 1,4-dioxane / 5 h / 20 °C

5: N-chloro-succinimide / N,N-dimethyl-formamide / 20 °C

6: water; lithium hydroxide / tetrahydrofuran; methanol / 70 °C

7: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogenchloride; N-chloro-succinimide; water; ammonium formate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; lithium hydroxide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 796870-83-2
1-(1,1-dimethylethyl) 2-ethyl 5-[(phenylmethyl)oxy]-1H-indole-1,2-dicarboxylate

: 1093256-33-7
N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: ammonium formate / palladium on activated charcoal

2: triphenylphosphine / dichloromethane / 1 h / 45 °C

3: hydrogenchloride / tetrahydrofuran; 1,4-dioxane / 5 h / 20 °C

4: N-chloro-succinimide / N,N-dimethyl-formamide / 20 °C

5: water; lithium hydroxide / tetrahydrofuran; methanol / 70 °C

6: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogenchloride; N-chloro-succinimide; water; ammonium formate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; lithium hydroxide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;