N-(3-methoxyphenyl)piperazine → HCID 66576861, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8]2[C:12]([C:13]([OH:15])=O)=[C:11]([CH3:16])[O:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1.Cl.C(N=C=NCCCN(C)C)C.[CH3:29][O:30][C:31]1[CH:32]=[C:33]([N:37]2[CH2:42][CH2:41][NH:40][CH2:39][CH2:38]2)[CH:34]=[CH:35][CH:36]=1>ClCCl>[F:1][C:2]1[CH:3]=[C:4]([C:8]2[C:12]([C:13]([N:40]3[CH2:39][CH2:38][N:37]([C:33]4[CH:34]=[CH:35][CH:36]=[C:31]([O:30][CH3:29])[CH:32]=4)[CH2:42][CH2:41]3)=[O:15])=[C:11]([CH3:16])[O:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In a similar manner as described in Example 1, by using dichloromethane (30 mL), 3-(3-fluorophenyl)-5-methylisoxazol-4-carboxylic acid (407 mg, 1.84 mmol), 1-ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride (388 mg, 2.02 mmol) and 1-(3-methoxyphenyl)piperazine (354 mg, 1.84 mmol), a white solid required compound (612 mg, 1.55 mmol, 84%) was obtained.
Sources & evidence
- ORD record
- ord-f894c00c80154ef083ba30fd7abc06cc
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09132126B2
Reaction notes
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