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Chemical Structure| 3682-14-2 Chemical Structure| 3682-14-2
Chemical Structure| 3682-14-2
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Product Details of Isoluminol

CAS No. :3682-14-2
Formula : C8H7N3O2
M.W : 177.16
SMILES Code : O=C1NNC(C2=C1C=CC(N)=C2)=O
Synonyms :
4-Aminophthalhydrazide
MDL No. :MFCD00010560
InChI Key :HUDPLKWXRLNSPC-UHFFFAOYSA-N
Pubchem ID :95014

Safety of Isoluminol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Isoluminol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 3682-14-2 ]

[ 3682-14-2 ] Synthesis Path-Downstream   1~23

  • 1
  • [ 2518-24-3 ]
  • [ 3682-14-2 ]
  • 3
  • [ 3682-19-7 ]
  • [ 3682-14-2 ]
YieldReaction ConditionsOperation in experiment
85% With palladium 10% on activated carbon; hydrogen; at 35℃; under 3040.2 Torr; for 4h; Transfer the product B to a 5 L hydrogenation vessel, add 3 g of 10 wtpercent palladium on carbon palladium, heat to 35 ° C, while the introduction of hydrogen pressure to 4atm, continue to heat constant pressure reaction 4 hours, after the end of the reaction, the hydrogen into nitrogen, Adjust the pH to 3-4 with 35 wtpercent concentrated hydrochloric acid, continue heating to 100 ° C, stop the introduction of nitrogen, filter hot, and cool the filtrate to HTC, a large number of precipitated precipitation, precipitate out completely after the filter, the filtrate for organic solvent recovery, filter cake with 400ml deionized water washing, drying, to be 214g isluminolide (4-amino phthalide)
26 g With sodium thiosulfate; In ethanol; for 3h;Reflux; Under stirring at room temperature, in a step upward reaction to the 10g sodium thiosulfate, after stirring at room temperature for 30 minutes. Then heating reflux reaction 3 hours, confirming board 4-nitrosodi phthalic hydrazide has been fully converted to the required products, to stop the reaction, the reaction liquid natural cooling down to room temperature, then filtered, collecting filter cake. Filtrate the spin vaporization recovery 95percent ethanol, the residue combined with the filter cake, is added to the 200 ml water, heating to 80 °C, stirring 30 minutes, there are still some solid insoluble, filter when it is hot. In the filtrate by adding concentrated hydrochloric acid to adjust pH to 9, natural cooling crystallization. Filtering, receive 26g strawcoloured powdered products.
  • 4
  • [ 2307-00-8 ]
  • [ 3682-14-2 ]
  • 7
  • N.N'-<4-nitro-phthalyl>-hydrazine [ No CAS ]
  • [ 3682-14-2 ]
  • 8
  • [ 7647-01-0 ]
  • [ 3682-14-2 ]
  • [ 99-05-8 ]
  • 10
  • [ 3682-14-2 ]
  • [ 214476-71-8 ]
  • 4-(1,4-dioxo-1,2, 3,4-tetrahydro-phthalazin-6-ylamino)-6,7-diethoxy-quinoline-3-carbonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
A solution of 400 mg (1.44 mM) of 4-chloro-6,7-diethoxy-quinoline-3-carbonitrile and 273 mg (1.54 mM) of 4-Aminophthalhydrazide Hydrate in 15 ml of 2-methoxyethanol was refluxed for 3 hours. To the warm solution was added 1 ml of 1M sodium carbonate and the sample was heated for 5 minutes at 100C, then poured into 300 ml of ice water. The solution was made acetic by addition of concentrated HCl and the solid was collected, washed with water followed by ether and dried under vacuum at 80C. The solid was taken up into 200 ml of methanol and 500l of 5 N sodium hydroxide and boiled for 20 minutes. To this heterogeneous mixture was added 100 ml of glacial acetic acid and the volume was reduced to a total of 100 ml by boiling. To the room temperature mixture, 500 ml of ice cold water was added and the solid was collected, washed with water followed by ether and dried under vacuum at 80C. The solid was digested in 400 ml of ethanol until the volume had been reduced to 150 ml. The hot solution was filtered and the solid was washed with ethanol and to dried under vacuum at 80C yield 121 mg of the title compound as a white solid: mass spectrum (electrospray, m/e): M+H 418.0, mp = >270C.
  • 11
  • [ 463-71-8 ]
  • [ 3682-14-2 ]
  • isoluminol isothiocyanate [ No CAS ]
  • 12
  • [ 3676-85-5 ]
  • [ 3682-14-2 ]
  • 13
  • [ 3682-14-2 ]
  • 4-azidophthalhydrazide [ No CAS ]
  • 14
  • [ 4418-61-5 ]
  • [ 3682-14-2 ]
  • [ 5970-45-6 ]
  • [Zn2(4-aminophthalic acid(-2H))(5-aminotetrazolate)2] [ No CAS ]
  • 15
  • [ 3682-14-2 ]
  • [ 1050602-61-3 ]
  • 6-((4-(cyclopropylamino)-5-(trifluoromethyl)pyrimidin-2-yl)amino)-2,3-dihydrophthalazine-1,4-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
35 mg With acetic acid; at 110℃; for 0.333333h;Microwave irradiation; Example 334: Preparation of 6-((4-(cyclopropyIamino)-5-(trifluoromethyl)pyrimidin-2- yl)amino)-2,3-dihydrophthalazine-l,4-dione2-Chloro-N-cyclopropyl-5-(trifluoromethyl)pyrimidin-4-amine (0.055 g, 0.231 mmol) and 6-amino-2,3-dihydrophthalazine-1 ,4-dione (0.041 g, 0.231 mmol) were mixed in acetic acid (2 ml). The mixture was microwaved at 1 10 °C for 20 min and then concentrated. Added MeOH and 5percent DMF and filtered the solid to give 35 mg of product. MS calcd for [Ci6H13F3N602+H]+: 379.12, found 379.00.
  • 16
  • [ 1445-69-8 ]
  • [ 3682-14-2 ]
  • 17
  • [ 3069-13-4 ]
  • [ 3682-14-2 ]
  • 18
  • [ 3682-14-2 ]
  • [ 122775-35-3 ]
  • [ 298-12-4 ]
  • [ 960232-00-2 ]
  • 19
  • [ 3682-14-2 ]
  • [ 122775-35-3 ]
  • methyl 3-(1-(2-(3,4-dimethoxyphenyl)-2-(1,4-dioxo-1,2,3,4-tetrahydrophthalazin-6-ylamino)acetyl)pyrrolidin-2-yl)-4-(isopropylsulfonyl)phenylcarbamate [ No CAS ]
  • 20
  • [ 89-40-7 ]
  • [ 3682-14-2 ]
  • 21
  • [ 3682-14-2 ]
  • C12H13N5O4 [ No CAS ]
  • 22
  • [ 108-30-5 ]
  • [ 3682-14-2 ]
  • C12H11N3O5 [ No CAS ]
  • 23
  • [ 108-55-4 ]
  • [ 3682-14-2 ]
  • C13H13N3O5 [ No CAS ]
 

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