Diisopropylethylamine → Methyl 2-amino-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate

HRID 874428Notes

Reaction equation

HRID 874428 reaction equation
C(OC([N:6]=[C:7]=S)=O)C.[CH3:9][O:10][C:11]([C:13]1[CH:18]=[CH:17][N:16]=[C:15]([NH2:19])[CH:14]=1)=[O:12].Cl.ON.C([N:26](C(C)C)CC)(C)C>C(O)C.CO.O1CCOCC1>[NH2:26][C:7]1[N:19]=[C:15]2[CH:14]=[C:13]([C:11]([O:10][CH3:9])=[O:12])[CH:18]=[CH:17][N:16]2[N:6]=1

Participants

8

Procedure

Ethoxycarbonyl isothiocyanate (9.0 g) was added to a 1,4-dioxane (100 ml) suspension of 2-aminopyridine-4-carboxylic acid methyl ester (10 g) at an internal temperature of 19° C. to 23° C. over 20 minutes. The obtained mixture was stirred for 90 minutes at the same temperature as described above, and was then concentrated under reduced pressure to obtain a crude product. The obtained crude product was added to a mixed suspension of methanol (70 ml) and ethanol (70 ml) containing hydroxyamine hydrochloride (22.8 g) and diisopropylethylamine (34 ml), and thereafter, the reaction solution was stirred at room temperature for 67 hours, at 60° C. for 5 hours, and again, at room temperature for 20 hours. Thereafter, the generated solid was collected, and it was washed with ethanol (30 ml) and was then dried, so as to obtain the title compound (11.3 g) in the form of a white solid.

Workup

  1. concentrationwas then concentrated under reduced pressure
  2. customto obtain a crude product
  3. customThe obtained crude product
  4. stirringthe reaction solution was stirred at room temperature for 67 hours, at 60° C. for 5 hours
  5. waitagain, at room temperature for 20 hours
  6. customThereafter, the generated solid was collected
  7. washit was washed with ethanol (30 ml)
  8. customwas then dried

Sources & evidence

ORD record
ord-5e47384374c44445af7f3a5a0678c13e
Source dataset
uspto-grants-2015_03
Patent number
US08980889B2

Reaction notes

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