HCID 86725599, compound → HCID 86725600, compound

HRID 514480Notes

Reaction equation

HRID 514480 reaction equation
[OH:1][C:2]1[N:6]([C:7]2[CH:12]=[C:11]([C:13]#[N:14])[CH:10]=[CH:9][N:8]=2)[N:5]=[CH:4][CH:3]=1.[CH3:15][CH:16]([O:19][C:20]1[CH:25]=[C:24]([Cl:26])[CH:23]=[CH:22][C:21]=1[CH2:27]O)[CH2:17][CH3:18]>>[CH3:15][CH:16]([O:19][C:20]1[CH:25]=[C:24]([Cl:26])[CH:23]=[CH:22][C:21]=1[CH2:27][O:1][C:2]1[N:6]([C:7]2[CH:12]=[C:11]([C:13]#[N:14])[CH:10]=[CH:9][N:8]=2)[N:5]=[CH:4][CH:3]=1)[CH2:17][CH3:18]

Participants

3

Procedure

The title compound was prepared from 2-(5-hydroxy-1H-pyrazol-1-yl)pyridine-4-carbonitrile and (2-butan-2-yloxy-4-chlorophenyl)methanol according to the procedure for the preparation of Example 39, part C. [M+H] Calc'd for C20H19ClN4O2, 383. Found, 383.

Sources & evidence

ORD record
ord-eddb5ebfce3d4f82bf349ebf8af627d7
Source dataset
uspto-grants-2015_08
Patent number
US09107916B2

Reaction notes

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