Propylamine → HCID 86738232, compound

HRID 1446905Notes

Reaction equation

HRID 1446905 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.[CH2:24]([NH2:27])[CH2:25][CH3:26]>>[ClH:2].[ClH:1].[ClH:2].[CH2:24]([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][CH2:16][CH2:15][CH3:14])[CH:15]=1)[CH:10]=2)[CH2:25][CH3:26]

Participants

3

Procedure

The compound is prepared from 3,6-bis(2-chloroethoxy)acridine hydrochloride and n-propylamine as described in Example 15, giving 1.20 g. of the desired product as yellow crystals, m.p. 250°-252° C.

Workup

  1. customgiving 1.20 g

Sources & evidence

ORD record
ord-5c34036b12be45a0aae66e703ad5e88f
Source dataset
uspto-grants-1982_02
Patent number
US04314061

Reaction notes

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