Diisopropylethylamine → HCID 25067121, compound

HRID 387066Notes

Reaction equation

HRID 387066 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[N:11]=[C:10]([CH2:19][CH2:20][CH:21]=O)[CH:9]=2)=[CH:4][CH:3]=1.[CH3:23][O:24][C:25]1[CH:30]=[CH:29][C:28]([N:31]2[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]2)=[CH:27][CH:26]=1.CCN(C(C)C)C(C)C.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:12]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[N:11]=[C:10]([CH2:19][CH2:20][CH2:21][N:34]3[CH2:35][CH2:36][N:31]([C:28]4[CH:27]=[CH:26][C:25]([O:24][CH3:23])=[CH:30][CH:29]=4)[CH2:32][CH2:33]3)[CH:9]=2)=[CH:6][CH:7]=1

Participants

5

Reactant 4

HCID 81531DiisopropylethylamineHCID 2697221-(4-Methoxyphenyl)piperazineHCID 5049666Sodium triacetoxyborohydrideHCID 866399223-(5-(4-chlorophenyl)-1-phenyl-1H-pyrazol-3-yl)-propanal

Product 1

HCID 25067121HCID 25067121, compound

Procedure

85 mg (63%) of target compound was obtained by using a method same as in Example 1 by using 3-(5-(4-chlorophenyl)-1-phenyl-1H-pyrazol-3-yl)-propanal (80 mg, 0.257 mmol), 1-(4-methoxyphenyl)piperazine (50 mg, 0.257 mmol), DIPEA (0.070 mL, 0.386 mmol) and NaBH(OAc)3 (163 mg, 0.771 mmol).

Workup

  1. custom85 mg (63%) of target compound was obtained

Sources & evidence

ORD record
ord-4c5d97254fa744e989d37a9e0dadeef5
Source dataset
uspto-grants-2013_02
Patent number
US08372844B2

Reaction notes

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