Isopropylamine → HCID 20553428, compound

HRID 1446908Notes

Reaction equation

HRID 1446908 reaction equation
[ClH:1].[Cl:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]2[C:18]([CH:19]=1)=[N:17][C:16]1[C:11](=[CH:12][CH:13]=[C:14]([O:20][CH2:21][CH2:22]Cl)[CH:15]=1)[CH:10]=2.[CH:24]([NH2:27])([CH3:26])[CH3:25]>>[ClH:2].[ClH:1].[ClH:2].[CH:24]([NH:27][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]2[C:18]([CH:19]=1)=[N:17][C:16]1[C:11](=[CH:12][CH:13]=[C:14]([O:20][CH2:21][CH2:22][NH:17][CH:16]([CH3:11])[CH3:15])[CH:15]=1)[CH:10]=2)([CH3:26])[CH3:25]

Participants

3

Reactant 2

HCID 6363IsopropylamineHCID 201846653,6-Bis(2-chloroethoxy)acridine--hydrogen chloride (1/1)

Product 1

HCID 20553428HCID 20553428, compound

Procedure

The compound is prepared from 3,6-bis(2-chloroethoxy)acridine hydrochloride and isopropylamine as described in Example 15, giving 1.1 g. of the desired product as yellow crystals, m.p. 232°-234° C.

Workup

  1. customgiving 1.1 g

Sources & evidence

ORD record
ord-eea7ce40942f4551a621b169ea9aa36f
Source dataset
uspto-grants-1982_02
Patent number
US04314061

Reaction notes

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