1H-Imidazole-1-pentanamine → HCID 178477836, compound

HRID 1090222Notes

Reaction equation

HRID 1090222 reaction equation
[Cl:1][C:2]1[C:3]2[C:4]3[C:8](=[CH:9][CH:10]=1)[N:7]=[C:6](S)[C:5]=3[CH:12]=[CH:13][CH:14]=2.[N:15]1([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][NH2:25])[CH:19]=[CH:18][N:17]=[CH:16]1>C(O)C>[Cl:1][C:2]1[C:3]2[C:4]3[C:8](=[CH:9][CH:10]=1)[N:7]=[C:6]([NH:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][N:15]1[CH:19]=[CH:18][N:17]=[CH:16]1)[C:5]=3[CH:12]=[CH:13][CH:14]=2

Participants

4

Reactant 2

HCID 71384341H-Imidazole-1-pentanamineHCID 178527785HCID 178527785, compound

Product 1

HCID 178477836HCID 178477836, compoundYield 76.8%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 4.4 g of 6-chloro-benz(cd)indole-2-thiol, 3.06 g of 5-(1H-imidazol-l-yl)pentanamine, 6.3 g of mercuric acetate and 150 ml of ethanol was reacted as described in Example 1, giving 5.2 g of the desired product, mp 132° C.-134° C.

Workup

  1. customwas reacted

Sources & evidence

ORD record
ord-76cf91a408c3484c85f7ef6494213edb
Source dataset
uspto-grants-1992_01
Patent number
US05081131

Reaction notes

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