Hydrochloric Acid → HCID 178478516, compound

HRID 1090211Notes

Reaction equation

HRID 1090211 reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])[CH:5]=[CH:4][N:3]=[CH:2]1.I.CS[C:18]1[C:26]2[CH:27]=[CH:28][CH:29]=[C:24]3[C:25]=2[C:20](=[CH:21][CH:22]=[CH:23]3)[N:19]=1.[ClH:30]>C(O)C>[ClH:30].[ClH:30].[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][NH:14][C:18]2[C:26]3[CH:27]=[CH:28][CH:29]=[C:24]4[C:25]=3[C:20](=[CH:21][CH:22]=[CH:23]4)[N:19]=2)[CH:5]=[CH:4][N:3]=[CH:2]1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 139528611H-Imidazole-1-octanamineHCID 201506502-Methylthiobenz(cd)indole hydriodide

Product 1

HCID 178478516HCID 178478516, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 2.1 of 8-(1H-imidazol-l-yl)octanamine, 400 ml of ethanol, and 3.2 g of 2-(methylthio)benz(cd)indole hydriodide was reacted as described in Example 19, giving the base derivative which was then treated with hydrochloric acid giving 1.3 g of the desired hydrochloride salt, mp 222° C.-224° C.

Workup

  1. customwas reacted
  2. customgiving the base derivative which

Sources & evidence

ORD record
ord-4f0d51a476ee4fbd97c5340365fe7601
Source dataset
uspto-grants-1992_01
Patent number
US05081131

Reaction notes

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