3,4-Dimethoxyaniline → HCID 56553438, compound

HRID 1593521Notes

Reaction equation

HRID 1593521 reaction equation
Cl[C:2]1[S:3][C:4]2[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[CH:7][C:5]=2[N:6]=1.[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:20]=[CH:21][C:22]=1[O:23][CH3:24])[NH2:19]>>[CH3:14][O:15][C:16]1[CH:17]=[C:18]([NH:19][C:2]2[S:3][C:4]3[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[CH:7][C:5]=3[N:6]=2)[CH:20]=[CH:21][C:22]=1[O:23][CH3:24]

Participants

3

Reactant 2

HCID 227703,4-DimethoxyanilineHCID 754762-Chloro-6-nitrobenzothiazole

Product 1

HCID 56553438HCID 56553438, compound

Procedure

The title compound was synthesised from 2-Chloro-6-nitro-benzothiazole (commercially available) and 3,4-dimethoxyaniline (commercially available) according to the procedure described for Example 1a) above. MS (m/e): 332.2 (MH+, 100%).

Sources & evidence

ORD record
ord-d74f313013574a3c98bbf6c0f56fcfb0
Source dataset
uspto-grants-2007_11
Patent number
US07297707B2

Reaction notes

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