(3-Chloro-4-ethylphenyl)methanol → 2-[5-[(3-Chloro-4-ethylphenyl)methoxy]pyrazol-1-yl]pyridine-4-carbonitrile

HRID 514441ノート

反応式

HRID 514441 の反応式
[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.[Cl:15][C:16]1[CH:17]=[C:18]([CH2:24]O)[CH:19]=[CH:20][C:21]=1[CH2:22][CH3:23]>>[Cl:15][C:16]1[CH:17]=[C:18]([CH2:24][O:1][C:2]2[N:6]([C:7]3[CH:12]=[C:11]([C:13]#[N:14])[CH:10]=[CH:9][N:8]=3)[N:5]=[CH:4][CH:3]=2)[CH:19]=[CH:20][C:21]=1[CH2:22][CH3:23]

参加物

3

反応物 2

HCID 86725560(3-Chloro-4-ethylphenyl)methanolHCID 178510213HCID 178510213、化合物

生成物 1

HCID 867255612-[5-[(3-Chloro-4-ethylphenyl)methoxy]pyrazol-1-yl]pyridine-4-carbonitrile

実験手順

The title compound was prepared from 2-(5-hydroxy-1H-pyrazol-1-yl)pyridine-4-carbonitrile and (3-chloro-4-ethylphenyl)methanol according to the procedure for the preparation of Example 39, part C. 1H NMR (400 MHz, CDCl3): δ 1.23 (3H, t, J=8.0 Hz), 2.76 (2H, t, J=8.0 Hz), 5.18 (2H, s), 5.74 (1H, d, J=0.8 Hz), 7.26 (2H, s), 7.40-7.44 (2H, m), 7.57 (1H, s), 8.03 (1H, s), 8.72 (1H, d, J=4.8 Hz). [M+H] Calc'd for C18H15ClN4O, 339. Found, 339.

出典と根拠

ORDレコード
ord-fab3f50824a14895bf774a542276b5bb
出典データセット
uspto-grants-2015_08
特許番号
US09107916B2

反応ノート

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