3-(5-methyl-1H-tetrazol-1-yl)aniline → HCID 46183428, compound

HRID 1880302Notes

Reaction equation

HRID 1880302 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][C:16]2[CH:21]=[CH:20][C:19](C3ON=CC=3)=[CH:18][CH:17]=2)[C:12]([C:27]([NH2:29])=[O:28])=[CH:11][N:10]=1.[CH3:30][C:31]1[N:35](C2C=C(C=CC=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:16]2[CH:17]=[CH:18][CH:19]=[C:20]([N:32]3[C:31]([CH3:30])=[N:35][N:34]=[N:33]3)[CH:21]=2)[C:12]([C:27]([NH2:29])=[O:28])=[CH:11][N:10]=1

Participants

3

Reactant 2

HCID 2526403-(5-methyl-1H-tetrazol-1-yl)anilineHCID 461846122-[[(1R,2S)-2-aminocyclohexyl]amino]-4-[4-(1,2-oxazol-5-yl)anilino]pyrimidine-5-carboxamide

Product 1

HCID 46183428HCID 46183428, compound

Procedure

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

Workup

  1. customThis compound was synthesised

Sources & evidence

ORD record
ord-2f33b0e0b95f48c786fbb22562b8042e
Source dataset
uspto-grants-2012_11
Patent number
US08318755B2

Reaction notes

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