Diisopropylethylamine → 5,7-Dichloro-[1,2,4]triazolo[1,5-A]pyridin-2-amine

HRID 712193Notes

Reaction equation

HRID 712193 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([NH:9][C:10]([NH:12]C(=O)OCC)=S)[CH:3]=1.Cl.NO.CC[N:23](C(C)C)C(C)C>CO.CCO>[Cl:8][C:6]1[N:5]2[N:23]=[C:10]([NH2:12])[N:9]=[C:4]2[CH:3]=[C:2]([Cl:1])[CH:7]=1

Participants

5

Procedure

Ethyl [(4,6-dichloropyridin-2-yl)carbamothioyl]carbamate (2.9 g, 9.9 mmol) was added to a stirred suspension of hydroxylamine hydrochloride (1.1 g, 16 mmol) and DIEA (1.9 g, 15 mmol) in MeOH/EtOH (1:1, 40 mL) portion-wise as a solid. This mixture was stirred at rt for 2 h and then heated at 80° C. for 18 h. The reaction mixture was concentrated in vacuo and the resultant reside treated with water yielding a cream solid, which was filtered and dried in a vacuum oven at 40° C. for 18 h to give the desired product (1.2 g, 60%). 1H NMR (DMSO) δ 7.58 (d, J=2.0 Hz, 1H), 7.35 (d, J=2.0 Hz, 1H), 6.44 (s, 2H). m/z [M+H]+=203.15.

Workup

  1. temperatureheated at 80° C. for 18 h
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. additionthe resultant reside treated with water yielding a cream solid, which
  4. filtrationwas filtered
  5. customdried in a vacuum oven at 40° C. for 18 h

Sources & evidence

ORD record
ord-143d166e301e4195b9249b690e8e7f2f
Source dataset
uspto-grants-2015_11
Patent number
US09181234B2

Reaction notes

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