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2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide

Base Information
  • Chemical Name:2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide
  • CAS No.:1448039-40-4
  • Molecular Formula:C21H23FN2O4S2
  • Molecular Weight:450.555
  • Hs Code.:
2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide

Synonyms:2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide

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Chemical Property of 2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide
Chemical Property:
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Technology Process of 2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide

There total 10 articles about 2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-amine 1',1'-dioxide 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:
Multi-step reaction with 8 steps
1.1: lithium diisopropyl amide / tetrahydrofuran; n-heptane; ethylbenzene / 0.25 h / -50 - -20 °C
1.2: -40 - 20 °C
2.1: trifluoroacetic acid / chloroform / 18 h / 0 - 50 °C
3.1: boron trifluoride diethyl etherate / tetrahydrofuran / 0.08 h / 0 °C
3.2: 3 h / 5 - 20 °C
4.1: triethylamine / 1,2-dichloro-ethane / 42 h / 80 °C
5.1: trifluoroacetic anhydride; urea hydrogen peroxide adduct / acetonitrile / 20 °C
6.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 2.5 h / 20 °C
7.1: acetic acid; nitric acid / 2 h / 20 °C
8.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 4.5 h / 20 °C
With palladium 10% on activated carbon; boron trifluoride diethyl etherate; hydrogen; nitric acid; urea hydrogen peroxide adduct; acetic acid; triethylamine; trifluoroacetic acid; trifluoroacetic anhydride; lithium diisopropyl amide; In tetrahydrofuran; ethanol; n-heptane; chloroform; ethylbenzene; ethyl acetate; 1,2-dichloro-ethane; acetonitrile; 1.1: |Wittig Olefination / 1.2: |Wittig Olefination / 2.1: |Fischer Indole Synthesis;
Guidance literature:
Multi-step reaction with 5 steps
1: triethylamine / 1,2-dichloro-ethane / 42 h / 80 °C
2: trifluoroacetic anhydride; urea hydrogen peroxide adduct / acetonitrile / 20 °C
3: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 2.5 h / 20 °C
4: acetic acid; nitric acid / 2 h / 20 °C
5: palladium 10% on activated carbon; hydrogen / ethyl acetate / 4.5 h / 20 °C
With palladium 10% on activated carbon; hydrogen; nitric acid; urea hydrogen peroxide adduct; acetic acid; triethylamine; trifluoroacetic anhydride; In tetrahydrofuran; ethanol; ethyl acetate; 1,2-dichloro-ethane; acetonitrile;
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