3-(4-Methyl-1-piperazine)propan-1-ol → 4-Chloro-7-methoxy-6-(3-(4-methylpiperazin-1-yl)propoxy)quinazoline

HRID 2108887Notes

Reaction equation

HRID 2108887 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:13][CH3:14])=[C:9]([OH:12])[CH:10]=2)[N:5]=[CH:4][N:3]=1.[CH3:15][N:16]1[CH2:21][CH2:20][N:19]([CH2:22][CH2:23][CH2:24]O)[CH2:18][CH2:17]1>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:13][CH3:14])=[C:9]([O:12][CH2:24][CH2:23][CH2:22][N:19]3[CH2:20][CH2:21][N:16]([CH3:15])[CH2:17][CH2:18]3)[CH:10]=2)[N:5]=[CH:4][N:3]=1

Participants

3

Reactant 2

HCID 792083-(4-Methyl-1-piperazine)propan-1-olHCID 231324754-Chloro-7-methoxyquinazolin-6-ol

Product 1

HCID 231324744-Chloro-7-methoxy-6-(3-(4-methylpiperazin-1-yl)propoxy)quinazoline

Procedure

The compound was synthesised according to GP 4 from 4-chloro-6-hydroxy-7-methoxy-quinazoline and 3-(4-methylpiperazin-1-yl)-propan-1-ol. LC/ESI-MS: m/z=351 [M+H].

Workup

  1. customThe compound was synthesised

Sources & evidence

ORD record
ord-004ce24f7d3a4bf7b55a07af64221b91
Source dataset
uspto-grants-2009_04
Patent number
US07514460B2

Reaction notes

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