2,6-Dimethylaniline → HCID 58692207, compound

HRID 2264258Notes

Reaction equation

HRID 2264258 reaction equation
[CH3:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:3]=1[NH2:4].C1(S([N:19]2[C:23]3=[N:24][CH:25]=[CH:26][CH:27]=[C:22]3[C:21]([C:28]3[CH:33]=[CH:32][N:31]=[C:30](Cl)[N:29]=3)=[CH:20]2)(=O)=O)C=CC=CC=1>>[CH3:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:3]=1[NH:4][C:30]1[N:29]=[C:28]([C:21]2[C:22]3[C:23](=[N:24][CH:25]=[CH:26][CH:27]=3)[NH:19][CH:20]=2)[CH:33]=[CH:32][N:31]=1

Participants

3

Reactant 2

HCID 68962,6-DimethylanilineHCID 59596028HCID 59596028, compound

Product 1

HCID 58692207HCID 58692207, compoundYield 40%

Procedure

Using the procedure of example 1, 2,6-dimethylaniline (98 mg) was reacted with compound 1f (100 mg) to provide compound 35 (34 mg, 40%). 1H NMR (400 MHz, CD3OD) δ 8.40 (d, J=8.0 Hz, 1H), 8.21 (d, J=4.8 Hz, 1H), 8.19 (s, 1H), 8.17 (d, J=5.2 Hz, 1H), 7.50 (d, J=7.2 Hz, 1H), 7.35 (d, J=7.2 Hz, 1H), 7.14 (d, J=5.2 Hz, 2H), 7.03 (t, J=5.2 Hz, 1H), 2.36 (s, 6H). MS (ESI) m/z: 316 (M+H)+.

Sources & evidence

ORD record
ord-1acfa6e573d544ada9f1f37d58b441b0
Source dataset
uspto-grants-2010_12
Patent number
US07855205B2

Reaction notes

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