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Chemical Structure| 53666-79-8

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Product Details of [ 53666-79-8 ]

CAS No. :53666-79-8
Formula : C3H5N3O
M.W : 99.09
SMILES Code : OC1=CC(N)=NN1
MDL No. :MFCD00233932
InChI Key :QZBGOTVBHYKUDS-UHFFFAOYSA-N
Pubchem ID :96221

Safety of [ 53666-79-8 ]

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

Application In Synthesis of [ 53666-79-8 ]

* 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 [ 53666-79-8 ]

[ 53666-79-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 934-48-5 ]
  • [ 53666-79-8 ]
  • [ 119769-05-0 ]
  • 2
  • [ 2516-33-8 ]
  • [ 53666-79-8 ]
  • [ 852443-66-4 ]
YieldReaction ConditionsOperation in experiment
15% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; DMF (N,N-dimethyl-formamide); at 25℃; Triphenylphosphine (16.0 g, 61 mmol),5-amino-2H-pyrazol-3-ol (5.5 g, 56 mmol), and cyclopropyl methanol (4.4 g, 61 mmol) were dissolved in THF (100 ml), to which was slowly added the diisopropyl azodicarboxylate (12 ml, 61 mmol) solution in THF (50 ml). The reaction mixture was stirred for 1 hour, diluted with DMF (45 ml), and allowed at25 C overnight. The solvent was removed under reduced pressure. The resulted residue was treated with water, extracted with EtOAc twice and DCM once. The combined organics were dried over anhydrous sodium sulfate, concentrated under reduced pressure, and purified by column chromatography (EtOAc) to give the title compound (1.3 g, 15%). MS: Calcd.: 153; Found: [M+H] + 154.
9% Referential Example 3 5-(Cyclopropylmethoxy)-lH-pyrazol-3 -amine (51) A mixture of Ph3P (75.5 g, 0.29 mol) and DIAD (58.5 g, 0.29 mol) in DCM (1.8 L) was stirred at RT for 30 min. The mixture was cooled to 0 C and 3 -amino-5 -hydroxy pyrazole (24.0 g, 0.24 mol) was added slowly over 10 min. After the addition was complete, the mixture was stirred at 0 C for 10 min, and cyclopropylmethanol (19.0 g, 0.265 mol) was added dropwise within 10 min at the same temperature. The mixture was stirred under RT for 48 h. The undissolved solid was filtered off, and the filtrate was concentrated to about 1 L. Aqueous HCl (25 mL con HCl in 70 mL water) was added to the solution until the pH was between 1 and 2. The solution was stirred for another 10 min and then H20 (350 mL) was added. After vigorous stirring for 30 min, the upper aqueous phase was separated and 20 g solid NaOH was added slowly to the aqueous phase until pH was ca. 9 to 11. The reaction mixture was extracted with EtOAc (6 x 300 mL) and the combined organic layers were dried (Na2S04), filtered and concentrated in vacuo. The crude product was purified by S1O2 column chromatography eluting with an EtO Ac/petroleum ether gradient (50 to 100% EtO Ac) affording 4.8 g of an oily product. Trituration with DCM (200 mL) and petroleum ether (250-300 mL) afforded 3.2 g (9%) of 51 as white to pale yellow solid: 1H NMR (400 MHz, DMSO-d6) δ 10.31 (m, 1H), 4.89 (m, 2H), 4.67 (s, 1H), 3.75 (d, J = 7.2 Hz, 2H), 1.24 - 1.11 (m, 1H), 0.52 - 0.50 (m, 2H), 0.30 - 0.15 (m, 2H); MS (ESI+) m/z = 154.0 [M +1]+.
 

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Related Functional Groups of
[ 53666-79-8 ]

Amines

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Related Parent Nucleus of
[ 53666-79-8 ]

Pyrazoles

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