HCID 473615, compound → HCID 59128865, compound

HRID 2390513Notes

Reaction equation

HRID 2390513 reaction equation
[NH:1]1[C:5]([C:6]2[S:10][C:9]([NH:11][C:12]3[C:13]([O:18][C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=4[C:25]([CH3:28])([CH3:27])[CH3:26])=[N:14][CH:15]=[CH:16][CH:17]=3)=[N:8][C:7]=2[C:29]([F:32])([F:31])[F:30])=[N:4][N:3]=[N:2]1.[CH3:33]N(CCCN=C(N)C1C=CC(C2NC(C3C=CC(C(N)=NCCCN(C)C)=CC=3)=CC=2)=CC=1)C>>[C:25]([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=1[O:18][C:13]1[C:12]([NH:11][C:9]2[S:10][C:6]([C:5]3[N:1]=[N:2][N:3]([CH3:33])[N:4]=3)=[C:7]([C:29]([F:31])([F:32])[F:30])[N:8]=2)=[CH:17][CH:16]=[CH:15][N:14]=1)([CH3:28])([CH3:26])[CH3:27]

Participants

3

Reactant 2

HCID 473615HCID 473615, compoundHCID 178440818HCID 178440818, compound

Product 1

HCID 59128865HCID 59128865, compound

Procedure

Example A133 was prepared from N-(5-(1H-tetrazol-5-yl)-4-(trifluoromethyl)thiazol-2-yl)-2-(2-tert-butylphenoxy)pyridin-3-amine (Example 404) following the procedure described for Example A132.

Sources & evidence

ORD record
ord-aab0c70f7ac345ed97a82d0a4090f214
Source dataset
uspto-grants-2012_09
Patent number
US08273772B2

Reaction notes

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