Potassium Carbonate → 3-Methyl-8-[6-(3-methyl-1,2,4-thiadiazol-5-yl)pyridazin-3-yl]-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one

HRID 2036079Notes

Reaction equation

HRID 2036079 reaction equation
Cl[C:2]1[N:3]=[N:4][C:5]([C:8]2[S:12][N:11]=[C:10]([CH3:13])[N:9]=2)=[CH:6][CH:7]=1.Cl.Cl.[CH3:16][N:17]1[C:21](=[O:22])[C:20]2([CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)[N:19]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH2:18]1.C(=O)([O-])[O-].[K+].[K+]>>[CH3:16][N:17]1[C:21](=[O:22])[C:20]2([CH2:23][CH2:24][N:25]([C:2]3[N:3]=[N:4][C:5]([C:8]4[S:12][N:11]=[C:10]([CH3:13])[N:9]=4)=[CH:6][CH:7]=3)[CH2:26][CH2:27]2)[N:19]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH2:18]1

Participants

4

Procedure

The object product (85 mg, 33%) was obtained in the same manner as in Example 1 and using 3-chloro-6-(3-methyl-1,2,4-thiadiazol-5-yl)pyridazine (130 mg), 3-methyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one dihydrochloride (223 mg) and potassium carbonate (130 mg).

Sources & evidence

ORD record
ord-91bcad9257c74adea0a243b5aaf564bc
Source dataset
uspto-grants-2013_11
Patent number
US08575167B2

Reaction notes

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