Hydrochloric Acid → 3-[(Ethyloxy)methyl]-1-(1-methylethyl)-1H-pyrazol-5-amine

HRID 1472567Notes

Reaction equation

HRID 1472567 reaction equation
[CH2:1]([O:3][CH2:4][C:5](=O)[CH2:6][C:7]#[N:8])[CH3:2].Cl.[CH:11]([NH:14][NH2:15])([CH3:13])[CH3:12].Cl>C(O)C>[CH2:1]([O:3][CH2:4][C:5]1[CH:6]=[C:7]([NH2:8])[N:14]([CH:11]([CH3:13])[CH3:12])[N:15]=1)[CH3:2]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 855731-Isopropylhydrazine hydrochlorideHCID 575169104-Ethoxy-3-oxobutanenitrile

Product 1

HCID 575169093-[(Ethyloxy)methyl]-1-(1-methylethyl)-1H-pyrazol-5-amineYield 65.6%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a 25 mL round bottom was added 4-(ethyloxy)-3-oxobutanenitrile (550 mg, 4.33 mmol), isopropyl hydrazine hydrochloride (478 mg, 4.33 mmol), and HCl (2.163 mL, 4.33 mmol) in Ethanol (10 mL). The reaction mixture was stirred at the room temperature overnight. The reaction mixture was then evaporated, and partitioned between 20 mL of ethyl acetate and 20 mL of 1 M Na2CO3. The organic layer was washed with brine, filtered and evaporated. 3-[(Ethyloxy)methyl]-1-(1-methylethyl)-1H-pyrazol-5-amine (520 mg, 2.84 mmol, 65.6% yield) was isolated as yellow oil. The product was used in the next step without further purification. 1H NMR (400 MHz, DMSO-d6) ppm 1.09 (t, J=7.07 Hz, 3 H) 1.26 (d, J=6.57 Hz, 6 H) 3.40 (q, J=6.91 Hz, 2 H) 4.16 (s, 2 H) 4.32 (quin, J=6.57 Hz, 1 H) 5.06 (s, 2 H) 5.22 (s, 1 H)

Workup

  1. customThe reaction mixture was then evaporated
  2. custompartitioned between 20 mL of ethyl acetate and 20 mL of 1 M Na2CO3
  3. washThe organic layer was washed with brine
  4. filtrationfiltered
  5. customevaporated

Sources & evidence

ORD record
ord-9c31f07cab6c4230930095f11d757b62
Source dataset
uspto-grants-2015_04
Patent number
US09012479B2

Reaction notes

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