635702-60-2

  • Product Name:2,3-dimethyl-2H-indazol-6-amine hydrochloride
  • Molecular Formula:C9H11N3.HCl
  • Purity:99%
  • Molecular Weight:197.667
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Product Details

Reputable Manufacturer Supply Reliable Quality 2,3-dimethyl-2H-indazol-6-amine hydrochloride 635702-60-2 Customized Supply

  • Molecular Formula:C9H11N3.HCl
  • Molecular Weight:197.667
  • PSA:43.84000 
  • LogP:2.84710 

2,3-dimethyl-2H-indazol-6-amine hydrochloride(Cas 635702-60-2) Usage

InChI:InChI=1/C9H11N3.ClH/c1-6-8-4-3-7(10)5-9(8)11-12(6)2;/h3-5H,10H2,1-2H3;1H

635702-60-2 Relevant articles

Method for preparing 2, 3-dimethyl-2H-indazole-6-benzylamine hydrochloride

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Paragraph 0029; 0034-0035; 0039; 0040; 0044-0045; 0049, (2020/03/14)

The invention discloses a method for pre...

Pyrimidineamines as angiogenesis modulators

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Paragraph 0178 - 0180, (2015/11/16)

Pyrimidine derivatives, which are useful...

Discovery of 5-[[4-[(2,3-dimethyl-2H-indazol-6-yl)methylamino]-2- pyrimidinyl]amino]-2-methyl-benzenesulfonamide (pazopanib), a novel and potent vascular endothelial growth factor receptor inhibitor

Harris, Philip A.,Boloor, Amogh,Cheung, Mui,Kumar, Rakesh,Crosby, Renae M.,Davis-Ward, Ronda G.,Epperly, Andrea H.,Hinkle, Kevin W.,Hunter III, Robert N.,Johnson, Jennifer H.,Knick, Victoria B.,Laudeman, Christopher P.,Luttrell, Deirdre K.,Mook, Robert A.,Nolte, Robert T.,Rudolph, Sharon K.,Szewczyk, Jerzy R.,Truesdale, Anne T.,Veal, James M.,Wang, Liping,Stafford, Jeffrey A.

experimental part, p. 4632 - 4640 (2009/06/18)

Inhibition of the vascular endothelial g...

Treatment Method

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Page/Page column 8-9, (2009/01/20)

The present invention is directed to met...

635702-60-2 Process route

2,3?dimethyl?6?nitro?2H?indazole
444731-73-1

2,3?dimethyl?6?nitro?2H?indazole

2,3-dimethyl-2H-indazole-6-amine hydrochloride
635702-60-2

2,3-dimethyl-2H-indazole-6-amine hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h;
96%
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h;
95%
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃;
95%
With tin(ll) chloride; hydrogenchloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h;
95%
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h; Inert atmosphere; Cooling with ice;
95%
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h;
95%
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h;
95%
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; at 0 ℃; for 0.583333h;
95%
With hydrogenchloride; tin(ll) chloride; In ethanol; water; at 0 ℃;
95%
3-methyl-6-nitro-1H-indazole
6494-19-5

3-methyl-6-nitro-1H-indazole

2,3-dimethyl-2H-indazole-6-amine hydrochloride
635702-60-2

2,3-dimethyl-2H-indazole-6-amine hydrochloride

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1.1: boron trifluoride diethyl etherate / dichloromethane / 0.25 h / -30 - 0 °C
1.2: 17.25 h / -70 - 20 °C
2.1: hydrogenchloride; tin(ll) chloride / diethylene glycol dimethyl ether; water / 0.58 h / 0 °C
With hydrogenchloride; boron trifluoride diethyl etherate; tin(ll) chloride; In dichloromethane; diethylene glycol dimethyl ether; water;
 
Multi-step reaction with 2 steps
1: sulfuric acid / dimethyl sulfoxide / 72 h / 50 °C
2: hydrogenchloride; tin(ll) chloride / diethylene glycol dimethyl ether; water / 0.58 h / 0 °C
With hydrogenchloride; sulfuric acid; tin(ll) chloride; In diethylene glycol dimethyl ether; water; dimethyl sulfoxide;
 
Multi-step reaction with 2 steps
1: acetone / 3 h / 20 °C
2: hydrogenchloride; tin(ll) chloride / diethylene glycol dimethyl ether; water / 0.58 h / 0 °C
With hydrogenchloride; tin(ll) chloride; In diethylene glycol dimethyl ether; water; acetone;
 
Multi-step reaction with 2 steps
1.1: boron trifluoride diethyl etherate / dichloromethane / 0.28 h / -30 - 0 °C
1.2: 17.25 h / -70 - 20 °C
2.1: hydrogenchloride; tin(ll) chloride / diethylene glycol dimethyl ether; water / 0.58 h / 0 °C
With hydrogenchloride; boron trifluoride diethyl etherate; tin(ll) chloride; In dichloromethane; diethylene glycol dimethyl ether; water;
 
Multi-step reaction with 2 steps
1: boron trifluoride diethyl etherate / dichloromethane / 17.53 h / -70 - 20 °C
2: hydrogenchloride; tin(ll) chloride / diethylene glycol dimethyl ether; water / 0.58 h / 0 °C
With hydrogenchloride; boron trifluoride diethyl etherate; tin(ll) chloride; In dichloromethane; diethylene glycol dimethyl ether; water;
 

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