HCID 3264560, compound → HCID 25100044, compound

HRID 574704Notes

Reaction equation

HRID 574704 reaction equation
[N:1]([C:4]1[S:5][C:6]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:7][C:8]=1[C:9]([O:11]C)=O)=[C:2]=[S:3].[CH3:19][C:20]1[N:24]([CH2:25][CH2:26][CH2:27][NH2:28])[CH:23]=[N:22][CH:21]=1>>[CH3:19][C:20]1[N:24]([CH2:25][CH2:26][CH2:27][N:28]2[C:9](=[O:11])[C:8]3[CH:7]=[C:6]([C:13]4[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=4)[S:5][C:4]=3[NH:1][C:2]2=[S:3])[CH:23]=[N:22][CH:21]=1

Participants

3

Reactant 2

HCID 3264560HCID 3264560, compoundHCID 194294833-(5-methyl-1H-imidazol-1-yl)propan-1-amine

Product 1

HCID 25100044HCID 25100044, compound

Procedure

The compound was synthesized starting from methyl 2-isothiocyanato-5-phenylthiophene-3-carboxylate (0.10 g, 0.36 mmol) and 3-(5-methyl-1H-imidazol-1-yl)propan-1-amine (5) (0.051 g, 0.36 mmol) as described above.

Workup

  1. customThe compound was synthesized

Sources & evidence

ORD record
ord-c71aa5fd8ce0400a8ee7455ffeee1a70
Source dataset
uspto-grants-2015_05
Patent number
US09034907B2

Reaction notes

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