p-(1-Piperazinyl)phenol → HCID 66576780, compound

HRID 2276435Notes

Reaction equation

HRID 2276435 reaction equation
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[C:13]([F:16])([F:15])[F:14])[C:3]=1[C:17]([OH:19])=O.Cl.C(N=C=NCCCN(C)C)C.OC1C2N=NNC=2C=CC=1.[N:42]1([C:48]2[CH:53]=[CH:52][C:51]([OH:54])=[CH:50][CH:49]=2)[CH2:47][CH2:46][NH:45][CH2:44][CH2:43]1>>[OH:54][C:51]1[CH:50]=[CH:49][C:48]([N:42]2[CH2:47][CH2:46][N:45]([C:17]([C:3]3[C:4]([C:7]4[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=4[C:13]([F:14])([F:15])[F:16])=[N:5][O:6][C:2]=3[CH3:1])=[O:19])[CH2:44][CH2:43]2)=[CH:53][CH:52]=1

Participants

5

Procedure

In a similar manner as described in Example 1, by using dimethylformimide (15 mL), 5-methyl-3-(2-(trifluoromethyl)phenyl)isoxazol-4-carboxylic acid (500 mg, 1.84 mmol), 1-ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride (388 mg, 2.02 mmol), hydroxybenzotriazole (299 mg, 2.21 mmol) and 4-(piperazine-1-yl)phenol (328 mg, 1.84 mmol), a white solid required compound (467 mg, 1.08 mmol, 59%) was obtained.

Sources & evidence

ORD record
ord-91eeb6c76f9242c5bc6e78b102b09f76
Source dataset
uspto-grants-2015_09
Patent number
US09132126B2

Reaction notes

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