Production Method 1

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Water ;  5 - 8 min, reflux

Reference

Microwave-assisted synthesis of new hydrazone compounds with two indole rings with antibacterial activities

Ye, Ying; Suo, You-rui; Yang, Fang; Yang, Yong-jing; Han, Li-juan, Huaxue Shiji, 2015, 37(7), 585-589

Production Method 2

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) ;  5 - 8 min, rt

Reference

Microwave-assisted synthesis and molecular recognition properties of novel indole acylhydrazone receptors

Ye, Ying; Suo, Yourui; Yang, Fang; Yang, Yongjing; Han, Lijuan, Journal of Chemical Research, 2015, 39(5), 296-299

Production Method 3

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) ;  10 min

Reference

Synthesis and antibacterial activities of novel 6-substituted indole derivatives containing 1,2,4-triazole Schiff base units promoted by microwave irradiation

Liu, Xing-li; Shi, Zhi-chuan; Zhao, Zhi-gang; Wang, Xiao-hong, Xinan Minzu Daxue Xuebao, 2014, 40(1), 44-48

Production Method 4

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Water ;  10 min, heated; cooled

Reference

Microwave-assisted synthesis of oxadiazoline derivatives containing indole structure and their antibacterial activities

Zhao, Zhigang; Liu, Xingli; Chen, Yu; Li, Hui; Shi, Zhichuan, Youji Huaxue, 2010, 30(12), 1949-1954

Production Method 5

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Water ;  10 min, heated

Reference

Synthesis and characterization of 3-acetyl-2-aryl-5-(6-indole)-1,3,4-oxadiazoline derivatives under microwave irradiation conditions

Ye, Ying; Zhao, Zhigang; Li, Qinghan; Chen, Yu, Huaxue Yanjiu Yu Yingyong, 2009, 21(9), 1340-1343

Production Method 6

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Water ;  10 min, heated

Reference

Microwave-assisted synthesis of indole-6-acylhydrazone and their antibacterial activities

Ye, Ying; Zhao, Zhigang; Liu, Xingli; Li, Qinghan, Youji Huaxue, 2009, 29(6), 993-997

Production Method 7

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine Solvents: Methanol ;  15 min

Reference

Microwave-assisted synthesis and characterization of indol-6-ylcarbohydrazones

Li, Qinghan; Zhao, Zhigang, Huaxue Yanjiu Yu Yingyong, 2008, 20(8), 988-991

Production Method 8

50820-65-0

851211-74-0

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1)

Reference

Synthesis and antibacterial activities of 6-substituted indole derivatives containing oxadiazole and sulfide units

Liu, Xing-li; Shi, Zhi-chuan; Zhao, Zhi-gang; Wang, Zhi-jing; Ye, Ying, Xinan Minzu Daxue Xuebao, 2013, 39(6), 877-880

1H-Indole-6-carbohydrazide Raw materials

• Methyl 1H-indole-6-carboxylate

1H-Indole-6-carbohydrazide Preparation Products

• 1H-Indole-6-carbohydrazide (851211-74-0)

• 1. 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
• 2. Evolution and characterization of a benzylguanine-binding RNA aptamer?
  J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
• 3. Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer?
  Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
• 4. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 5. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Indolecarboxamides and derivatives
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Indolecarboxylic acids and derivatives Indolecarboxamides and derivatives

• 321309-24-4(1H-Indole-7-carbohydrazide)
• 59282-61-0(3-Quinolinecarboxylic acid, hydrazide)
• 96541-83-2(Quinoline-5-carboxylic Acid Hydrazide)
• 1670-86-6(1H-Indole-4-carboxamide)
• 1670-88-8(1H-Indole-6-carboxamide)
• 1670-87-7(SD-169)
• 15317-58-5(1H-Indole-3-carbohydrazide)
• 36705-76-7(9-Acridinecarboxylicacid, hydrazide)
• 29620-62-0(Quinoline-4-carbohydrazide)
• 885272-22-0(1H-Indole-4-carbohydrazide)