HCID 68632008, compound → HCID 57829808, compound

HRID 1855390Notes

Reaction equation

HRID 1855390 reaction equation
CN(C)[CH:3]=[C:4]([C:8]1[O:12][N:11]=[C:10]([CH3:13])[N:9]=1)[C:5](=O)[CH3:6].[N+]([O-])(O)=O.[N+]([O-])(O)=O.[CH3:23][O:24][C:25]1[CH:26]=[C:27]([NH:37][C:38]([NH2:40])=[NH:39])[CH:28]=[CH:29][C:30]=1[N:31]1[CH:35]=[C:34]([CH3:36])[N:33]=[CH:32]1>>[CH3:23][O:24][C:25]1[CH:26]=[C:27]([NH:37][C:38]2[N:40]=[C:5]([CH3:6])[C:4]([C:8]3[O:12][N:11]=[C:10]([CH3:13])[N:9]=3)=[CH:3][N:39]=2)[CH:28]=[CH:29][C:30]=1[N:31]1[CH:35]=[C:34]([CH3:36])[N:33]=[CH:32]1

Participants

3

Reactant 2

HCID 68632008HCID 68632008, compoundHCID 178493228HCID 178493228, compound

Product 1

HCID 57829808HCID 57829808, compound

Procedure

The title compound was prepared from crude 4-dimethylamino-3-(3-methyl-[1,2,4]oxadiazol-5-yl)-but-3-en-2-one (313 mg, 1.6 mmol) and N-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-guanidine dinitrate (297 mg, 0.8 mmol) using in analogous manner the procedure described in example 39b). Obtained as a pale-yellow solid (142 mg, 47%).

Sources & evidence

ORD record
ord-ea21d87b0e754512a54d9eb9d1a98f22
Source dataset
uspto-grants-2015_02
Patent number
US08962834B2

Reaction notes

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