3-Chloro-2-(3-isopropoxy-4-methoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one → 3-Chloro-2-(3-isopropoxy-4-methoxyphenyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one

HRID 2097431Notes

Reaction equation

HRID 2097431 reaction equation
[Cl:1][C:2]1[C:10]2[C:9](=[O:11])[NH:8][N:7]=[CH:6][C:5]=2[N:4](COCC[Si](C)(C)C)[C:3]=1[C:20]1[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[C:22]([O:28][CH:29]([CH3:31])[CH3:30])[CH:21]=1.ClC1C2C(=O)NN=CC=2N(COCC[Si](C)(C)C)C=1C1C=CC(OC(F)F)=C(OC(C)C)C=1>>[Cl:1][C:2]1[C:10]2[C:9](=[O:11])[NH:8][N:7]=[CH:6][C:5]=2[NH:4][C:3]=1[C:20]1[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[C:22]([O:28][CH:29]([CH3:31])[CH3:30])[CH:21]=1

Participants

3

Procedure

Reaction and post treatment were carried out in the same manner as in Example 40-(b) except for using 305 mg (0.657 mmol) of 3-chloro-2-(3-isopropoxy-4-methoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one obtained in Example 48-(a) in place of 3-chloro-2-(4-difluoromethoxy-3-isopropoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one, whereby 164 mg of the title compound was obtained as a white solid. (Yield: 75%)

Workup

  1. customReaction and post treatment

Sources & evidence

ORD record
ord-2e8e51b988bd48e9b754abf7a7529f97
Source dataset
uspto-grants-2013_05
Patent number
US08450319B2

Reaction notes

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