3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)aniline → HCID 57471900, compound

HRID 559030Notes

Reaction equation

HRID 559030 reaction equation
[NH2:1][C@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[NH:8][C:9]1[N:14]=[C:13]([NH:15]C2C=CC(C3ON=CC=3)=CC=2)[C:12]([C:27]([NH2:29])=[O:28])=[CH:11][N:10]=1.[CH3:30][N:31]1[C:35]([C:36]2[CH:37]=[C:38]([CH:40]=[CH:41][CH:42]=2)N)=[N:34][N:33]=[N:32]1>>[NH2:1][C@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[NH:8][C:9]1[N:14]=[C:13]([NH:15][C:38]2[CH:40]=[CH:41][CH:42]=[C:36]([C:35]3[N:31]([CH3:30])[N:32]=[N:33][N:34]=3)[CH:37]=2)[C:12]([C:27]([NH2:29])=[O:28])=[CH:11][N:10]=1

Participants

3

Reactant 2

HCID 144576753-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)anilineHCID 461846122-[[(1R,2S)-2-aminocyclohexyl]amino]-4-[4-(1,2-oxazol-5-yl)anilino]pyrimidine-5-carboxamide

Product 1

HCID 57471900HCID 57471900, compound

Procedure

This compound was synthesised using the synthetic scheme described for the synthesis of compound 122, and using 3-(1-methyl-1H-tetrazol-5-yl)aniline in step 1. MS: 409.5 (M+H).

Workup

  1. customThis compound was synthesised

Sources & evidence

ORD record
ord-fb9d6e118be94f5b8d3293c9ab526589
Source dataset
uspto-grants-2011_11
Patent number
US08063058B2

Reaction notes

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