Methyl 2-isothiocyanato-4,5-dimethylthiophene-3-carboxylate → 2,3-dihydro-5,6-dimethyl-3-(3-(5-methyl-1H-imidazol-1-yl)propyl)-2-thioxothieno[2,3-d]pyrimidin-4(1H)-one

HRID 574702Notes

Reaction equation

HRID 574702 reaction equation
[N:1]([C:4]1[S:5][C:6]([CH3:14])=[C:7]([CH3:13])[C:8]=1[C:9]([O:11]C)=O)=[C:2]=[S:3].[CH3:15][C:16]1[N:20]([CH2:21][CH2:22][CH2:23][NH2:24])[CH:19]=[N:18][CH:17]=1>>[CH3:13][C:7]1[C:8]2[C:9](=[O:11])[N:24]([CH2:23][CH2:22][CH2:21][N:20]3[C:16]([CH3:15])=[CH:17][N:18]=[CH:19]3)[C:2](=[S:3])[NH:1][C:4]=2[S:5][C:6]=1[CH3:14]

Participants

3

Reactant 2

HCID 3459267Methyl 2-isothiocyanato-4,5-dimethylthiophene-3-carboxylateHCID 194294833-(5-methyl-1H-imidazol-1-yl)propan-1-amine

Product 1

HCID 251000422,3-dihydro-5,6-dimethyl-3-(3-(5-methyl-1H-imidazol-1-yl)propyl)-2-thioxothieno[2,3-d]pyrimidin-4(1H)-one

Procedure

The compound was synthesized starting from methyl 2-isothiocyanato-4,5-dimethylthiophene-3-carboxylate (0.1 g, 0.44 mmol) and 3-(5-methyl-1H-imidazol-1-yl)propan-1-amine (5) (0.06 g, 0.44 mmol) as described above.

Workup

  1. customThe compound was synthesized

Sources & evidence

ORD record
ord-2c80f7661d4a4ddca993bdbacac2e0a9
Source dataset
uspto-grants-2015_05
Patent number
US09034907B2

Reaction notes

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