HCID 4506508, compound → HCID 25100045, compound

HRID 574705Notes

Reaction equation

HRID 574705 reaction equation
[N:1]([C:4]1[S:8][C:7]2[CH2:9][CH2:10][CH2:11][C:6]=2[C:5]=1[C:12]([O:14]C)=O)=[C:2]=[S:3].[CH3:16][C:17]1[N:21]([CH2:22][CH2:23][CH2:24][NH2:25])[CH:20]=[N:19][CH:18]=1>>[CH3:16][C:17]1[N:21]([CH2:22][CH2:23][CH2:24][N:25]2[C:12](=[O:14])[C:5]3[C:6]4[CH2:11][CH2:10][CH2:9][C:7]=4[S:8][C:4]=3[NH:1][C:2]2=[S:3])[CH:20]=[N:19][CH:18]=1

Participants

3

Reactant 2

HCID 4506508HCID 4506508, compoundHCID 194294833-(5-methyl-1H-imidazol-1-yl)propan-1-amine

Product 1

HCID 25100045HCID 25100045, compound

Procedure

The compound was synthesized starting from methyl 5,6-dihydro-2-isothiocyanato-4H-cyclopenta[b]thiophene-3-carboxylate (0.10 g, 0.42 mmol) and 3-(5-methyl-1H-imidazol-1-yl)propan-1-amine (5) (0.058 g, 0.42 mmol) as described above.

Workup

  1. customThe compound was synthesized

Sources & evidence

ORD record
ord-c77c7b914cec41f5a1d6e55ff5897ed4
Source dataset
uspto-grants-2015_05
Patent number
US09034907B2

Reaction notes

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