3,4,5-Trimethoxyaniline → HCID 58639095, compound

HRID 548804Notes

Reaction equation

HRID 548804 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]([NH2:18])(=[O:17])=[O:16])[CH:5]=[CH:4][N:3]=1.[CH3:19][O:20][C:21]1[CH:22]=[C:23]([NH2:31])[CH:24]=[C:25]([O:29][CH3:30])[C:26]=1[O:27][CH3:28]>>[CH3:30][O:29][C:25]1[CH:24]=[C:23]([NH:31][C:2]2[N:7]=[C:6]([NH:8][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[S:15]([NH2:18])(=[O:17])=[O:16])[CH:5]=[CH:4][N:3]=2)[CH:22]=[C:21]([O:20][CH3:19])[C:26]=1[O:27][CH3:28]

Participants

3

Reactant 2

HCID 322853,4,5-TrimethoxyanilineHCID 86604889HCID 86604889, compound

Product 1

HCID 58639095HCID 58639095, compound

Procedure

The title compound is prepared from 2-(2-chloro-pyrimidin-4-ylamino)-benzenesulfonamide as described in Example 1 using 3,4,5-Trimethoxy-phenylamine instead of 6-aminoindazole in step (b).

Sources & evidence

ORD record
ord-88b87ac645c341d5bb3525a8285249bd
Source dataset
uspto-grants-2011_05
Patent number
US07943627B2

Reaction notes

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