2,4-Dichloro-5-methoxyaniline → N4-(2,4-dichloro-5-methoxyphenyl)-7-methoxyquinazoline-4,6-diamine

HRID 2205312Notes

Reaction equation

HRID 2205312 reaction equation
ClC1C=C(NC2C3C(=CC(OCCOC)=C(N)C=3)N=CN=2)C=CC=1F.Cl[C:27]1[C:36]2[C:31](=[CH:32][C:33]([O:40][CH3:41])=[C:34]([N+:37]([O-])=O)[CH:35]=2)[N:30]=[CH:29][N:28]=1.[Cl:42][C:43]1[CH:49]=[C:48]([Cl:50])[C:47]([O:51][CH3:52])=[CH:46][C:44]=1[NH2:45]>>[Cl:42][C:43]1[CH:49]=[C:48]([Cl:50])[C:47]([O:51][CH3:52])=[CH:46][C:44]=1[NH:45][C:27]1[C:36]2[C:31](=[CH:32][C:33]([O:40][CH3:41])=[C:34]([NH2:37])[CH:35]=2)[N:30]=[CH:29][N:28]=1

Participants

4

Reactant 3

HCID 14766362,4-Dichloro-5-methoxyanilineHCID 104901874-Chloro-7-methoxy-6-nitroquinazolineHCID 18765584N4-(3-Chloro-4-fluorophenyl)-7-(2-methoxyethoxy)quinazoline-4,6-diamine

Product 1

HCID 86727277N4-(2,4-dichloro-5-methoxyphenyl)-7-methoxyquinazoline-4,6-diamine

Procedure

Starting material: N4-(2,4-dichloro-5-methoxyphenyl)-7-methoxyquinazoline-4,6-diamine was prepared according to the same method of preparation of N4-(3-chloro-4-fluorophenyl)-7-(2-methoxy)ethoxyquinazoline-4,6-diamine in WO2008/33747, but the starting material was 4-chloro-7-methoxy-6-nitro-quinazoline and 2,4-dichloro-5-methoxyaniline; other starting materials were prepared as example 1.

Workup

  1. customother starting materials were prepared as example 1

Sources & evidence

ORD record
ord-b8129bda4e6c4c30a9c2f18c1f37816f
Source dataset
uspto-grants-2016_06
Patent number
US09371292B2

Reaction notes

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