Production Method 1

96187-75-6

Reaction Conditions

Reference

Preparation of 1,3-dihydro-2H-indol-2-ones with selective binding affinity for the V1b arginine-vasopressin receptor for pharmaceutical use

, World Intellectual Property Organization, , ,

Production Method 2

96187-75-6

Reaction Conditions

Reference

Synthesis of 3,4-dihydro-1,4-ethenonaphthalen-2(1H)-ones by benzyne cycloadditions

Ghisalberti, Emilio L.; Jefferies, Phillip R.; Mori, Trevor A.; Skelton, Brian W.; White, Allan H.; et al, Journal of Chemical Research, 1993, (12), 474-5

Production Method 3

155184-79-5

96187-75-6

53003-18-2

Reaction Conditions

1.1 Reagents: Sulfuric acid
1.2 Solvents: Acetic acid

Reference

Synthesis and In Vitro Antitumor Activity of Thiophene Analogues of 5-Chloro-5,8-dideazafolic Acid and 2-Methyl-2-desamino-5-chloro-5,8-dideazafolic Acid

Forsch, Ronald A.; Wright, Joel E.; Rosowsky, Andre, Bioorganic & Medicinal Chemistry, 2002, 10(6), 2067-2076

Production Method 4

96187-75-6

Reaction Conditions

Reference

Preparation and use of dihydroindolone derivatives as vasopressin receptor ligands

, World Intellectual Property Organization, , ,

Production Method 5

96187-75-6

Reaction Conditions

Reference

Novel 1,3-dihydro-2H-indol-2-ones, preparation, pharmaceutical compositions containing same and use for treating pathologies involving arginine-vasopressin receptors

, World Intellectual Property Organization, , ,

Production Method 6

96187-75-6

Reaction Conditions

Reference

Preparation of N-oxoindolylpyrrolidine-2-carboxamides and analogs as vasopressin V1a and V1b receptor ligands

, World Intellectual Property Organization, , ,

Production Method 7

155184-79-5

96187-75-6

53003-18-2

Reaction Conditions

1.1 Reagents: Sulfuric acid

Reference

Synthesis of thiazolo[2',3':3,4][1,2,4]triazino[5,6-b]indole from 4,5-disubstituted isatin

Saha, Goutam Kumar; Rashid, M. D. Abdur; Islam, M. D. Rabiul, Journal of the Bangladesh Chemical Society, 2000, 13, 47-51

6-Chloro-5-methylindoline-2,3-dione Raw materials

6-Chloro-5-methylindoline-2,3-dione Preparation Products

• 6-Chloro-5-methylindoline-2,3-dione (96187-75-6)
• 4-Chloro-5-methylisatin (53003-18-2)

• 1. Fc microparticles can modulate the physical extent and magnitude of complement activity?
  David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
• 2. Exchanged ligands on the surface of a giant cluster: [(MoO3)176(H2O)63(CH3OH)17Hn](32 – n)–
  Chem. Commun., 1998, 1501-1502
• 3. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 4. Exceptionally high temperature spin crossover in amide-functionalised 2,6-bis(pyrazol-1-yl)pyridine iron(ii) complex revealed by variable temperature Raman spectroscopy and single crystal X-ray diffraction?
  Max Attwood,Hiroki Akutsu,Lee Martin,Toby J. Blundell,Pierre Le Maguere,Scott S. Turner Dalton Trans., 2021,50, 11843-11851
• 5. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Indolines

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)