3,4,5-Trimethylbenzene-1,2-diamine → HCID 136492482, compound

HRID 59472Notes

Reaction equation

HRID 59472 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[NH:13][C:12](=[O:14])[N:11]([C:15]2[CH:24]=[CH:23][C:18]([C:19](OC)=O)=[C:17]([O:25][CH3:26])[CH:16]=2)[N:10]=1.[CH3:27][C:28]1[CH:33]=[C:32]([NH2:34])[C:31]([NH2:35])=[C:30](C)[C:29]=1[CH3:37].[CH3:38][Al](C)C>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[NH:13][C:12](=[O:14])[N:11]([C:15]2[CH:24]=[CH:23][C:18]([C:19]3[N:35]([CH3:38])[C:31]4[CH:30]=[C:29]([CH3:37])[C:28]([CH3:27])=[CH:33][C:32]=4[N:34]=3)=[C:17]([O:25][CH3:26])[CH:16]=2)[N:10]=1

Participants

5

Procedure

The title compound was prepared by following the procedure as described for Example-31 by using methyl 4-(3-(2-chloro-6-fluorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)-2-methoxybenzoate (step-2 of Intermediate-15, 0.100 g, 0.26 mmol), trimethylbenzene-1,2-diamine (Intermediate-31, 0.048 g, 0.32 mmol), trimethyl aluminium (2M solution in toluene) (0.5 mL), dry toluene (5.0 mL) to afford 0.030 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 2.33 (s, 3H), 2.36 (s, 3H), 3.56 (s, 3H), 3.85 (s, 3H), 7.33 (s, 1H), 7.41 (s, 1H), 7.47-7.59 (m, 3H), 7.66-7.78 (m, 3H), 12.5 (br s, 1H); MS (m/z): 478.29 (M+H+).

Workup

  1. customThe title compound was prepared

Sources & evidence

ORD record
ord-55fc9bd287d848129d42f4998ea263e1
Source dataset
uspto-grants-2016_09
Patent number
US09439890B2

Reaction notes

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