Potassium Carbonate → HCID 68554325, compound

HRID 2036116Notes

Reaction equation

HRID 2036116 reaction equation
Cl[C:2]1[N:3]=[N:4][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[N:9]=2)=[CH:6][CH:7]=1.[NH:14]1[CH2:18][CH2:17][C:16]2([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=3[C:20](=[O:27])[O:19]2)[CH2:15]1.C(=O)([O-])[O-].[K+].[K+]>>[CH3:13][C:10]1[N:9]=[C:8]([C:5]2[N:4]=[N:3][C:2]([N:14]3[CH2:18][CH2:17][C:16]4([C:22]5[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=5[C:20](=[O:27])[O:19]4)[CH2:15]3)=[CH:7][CH:6]=2)[O:12][N:11]=1

Participants

4

Reactant 3

HCID 11430Potassium CarbonateHCID 167322943-Chloro-6-(3-methyl-1,2,4-oxadiazol-5-yl)pyridazineHCID 215068143H-Spiro[2-benzofuran-1,3'-pyrrolidin]-3-one

Product 1

HCID 68554325HCID 68554325, compound

Procedure

The object product (10 mg, 6%) was obtained in the same manner as in Example 1 and using 3-chloro-6-(3-methyl-1,2,4-oxadiazol-5-yl)pyridazine (100 mg) obtained in Example 43(2), 3H-spiro[2-benzofuran-1,3′-pyrrolidin]-3-one (110 mg) and potassium carbonate (150 mg).

Sources & evidence

ORD record
ord-ee7d630434b34bc6b9da4f7ed8c60ddc
Source dataset
uspto-grants-2013_11
Patent number
US08575167B2

Reaction notes

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