3-(4-Methyl-1H-imidazol-1-yl)propan-1-amine → HCID 25100518, compound

HRID 574722Notes

Reaction equation

HRID 574722 reaction equation
[N:1]([C:4]1[S:5][C:6]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:7][C:8]=1[C:9]([O:11]C)=O)=[C:2]=[S:3].[CH3:20][C:21]1[N:22]=[CH:23][N:24]([CH2:26][CH2:27][CH2:28][NH2:29])[CH:25]=1>>[CH2:13]([C:6]1[S:5][C:4]2[NH:1][C:2](=[S:3])[N:29]([CH2:28][CH2:27][CH2:26][N:24]3[CH:25]=[C:21]([CH3:20])[N:22]=[CH:23]3)[C:9](=[O:11])[C:8]=2[CH:7]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

3

Reactant 2

HCID 150349543-(4-Methyl-1H-imidazol-1-yl)propan-1-amineHCID 19620644HCID 19620644, compound

Product 1

HCID 25100518HCID 25100518, compound

Procedure

The compound was synthesized starting from methyl 2-isothiocyanato-5-benzylthiophene-3-carboxylate (0.102 g. 0.35 mmol) and 3-(4-methyl-1H-imidazol-1-yl)propan-1-amine (0.049 g, 0.35 mmol) as described above.

Workup

  1. customThe compound was synthesized

Sources & evidence

ORD record
ord-88ef480c2219480f9c0f0d657bf3d50e
Source dataset
uspto-grants-2015_05
Patent number
US09034907B2

Reaction notes

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