Hexachloroethane → 4,5-Dimethyl-3-(5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-6-[4-(5-trifluoromethyl-pyridin-2-yl)-piperazin-1-yl]-pyridazine

HRID 447136Notes

Reaction equation

HRID 447136 reaction equation
[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([N:9]2[CH2:14][CH2:13][N:12]([C:15]3[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][N:16]=3)[CH2:11][CH2:10]2)[N:5]=[N:4][C:3]=1[CH2:25][C:26]([NH:28][NH:29][C:30](=O)[CH3:31])=[O:27].C(N(C(C)C)CC)(C)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.ClC(Cl)(Cl)C(Cl)(Cl)Cl>C(#N)C>[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([N:9]2[CH2:14][CH2:13][N:12]([C:15]3[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:22])[F:23])=[CH:17][N:16]=3)[CH2:11][CH2:10]2)[N:5]=[N:4][C:3]=1[CH2:25][C:26]1[O:27][C:30]([CH3:31])=[N:29][N:28]=1

Participants

6

Procedure

Acetic acid N′-(2-{4,5-dimethyl-6-[4-(5-trifluoromethyl-pyridin-2-yl)-piperazin-1-yl]-pyridazin-3-yl}-acetyl)-hydrazide (114 mg, 0.248 mmol) is added to a round-bottom flask under N2 followed by acetonitrile (3 mL), diisopropylethylamine (0.27 mL, 1.43 mmol) and triphenylphosphine (115.5 mg, 0.44 mmol) and the reaction is stirred for 30 min. Hexachloroethane (77.5 mg, 0.329 mmol) is then added and the reaction is stirred for 16 h. The crude mixture is purified via HPLC (ammonium hydroxide as a modifier) to afford the title compound (8 mg, 7%).

Workup

  1. stirringthe reaction is stirred for 16 h
  2. customThe crude mixture is purified via HPLC (ammonium hydroxide as a modifier)

Sources & evidence

ORD record
ord-312986a50c954ef295ab40e7a86c36d0
Source dataset
uspto-grants-2013_07
Patent number
US08481542B2

Reaction notes

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