HCID 66602776, compound → 2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-hydroxymethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one

HRID 2097383Notes

Reaction equation

HRID 2097383 reaction equation
[CH:1]1([O:4][C:5]2[CH:6]=[C:7]([C:15]3[N:24](COCC[Si](C)(C)C)[C:18]4[CH:19]=[N:20][NH:21][C:22](=[O:23])[C:17]=4[C:16]=3[CH2:33][OH:34])[CH:8]=[CH:9][C:10]=2[O:11][CH:12]([F:14])[F:13])[CH2:3][CH2:2]1>O>[CH:1]1([O:4][C:5]2[CH:6]=[C:7]([C:15]3[NH:24][C:18]4[CH:19]=[N:20][NH:21][C:22](=[O:23])[C:17]=4[C:16]=3[CH2:33][OH:34])[CH:8]=[CH:9][C:10]=2[O:11][CH:12]([F:13])[F:14])[CH2:2][CH2:3]1

Participants

3

Procedure

Reaction was carried out in the same manner as in Example 1-(b) except for using 80 mg (0.16 mmol) of 2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-hydroxymethyl-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Example 10-(b) in place of 2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one. After completion of the reaction, water was added to the reaction mixture and the precipitated solid was collected by filtration. The obtained solid was washed with water and dried under reduced pressure to obtain 50 mg of the title compound as a white solid. (Yield: 85%)

Workup

  1. customReaction
  2. additionwas added to the reaction mixture
  3. filtrationthe precipitated solid was collected by filtration
  4. washThe obtained solid was washed with water
  5. customdried under reduced pressure

Sources & evidence

ORD record
ord-408f6ad671f9496199c491ed2ee7e1b7
Source dataset
uspto-grants-2013_05
Patent number
US08450319B2

Reaction notes

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