1-Methyl-4-piperidinemethanol → 4-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline

HRID 2108897Notes

Reaction equation

HRID 2108897 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([OH:14])=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][N:3]=1.[CH3:15][N:16]1[CH2:21][CH2:20][CH:19]([CH2:22]O)[CH2:18][CH2:17]1>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH2:22][CH:19]3[CH2:20][CH2:21][N:16]([CH3:15])[CH2:17][CH2:18]3)=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][N:3]=1

Participants

3

Reactant 2

HCID 2719711-Methyl-4-piperidinemethanolHCID 1357422514-Chloro-6-methoxyquinazolin-7-ol

Product 1

HCID 117822304-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline

Procedure

The compound was synthesised according to GP 4 from 4-chloro-7-hydroxy-6-methoxy-quinazoline and (1-Methyl-piperidin-4-yl)-methanol. LC/ESI-MS: m/z=322 [M+H].

Workup

  1. customThe compound was synthesised

Sources & evidence

ORD record
ord-60d28210dc024d849f2db86e0a449fb2
Source dataset
uspto-grants-2009_04
Patent number
US07514460B2

Reaction notes

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