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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598896Generated: October 25, 2026

N-(4-Phenylpiperidin-4-yl)acetamide → 5-[(1RS,2RS)-2-(3,4-Dichlorophenyl)-1-hydroxy-4-(4-acetamido-4-phenylpiperidino)butyl]-1-phenylpyrazole

https://huagongshe.com/reaction/1598896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Phenylpiperidin-4-yl)acetamideHCID 15886675—
Reactant5-[(1RS,2RS)-1-acetoxy-2-(3,4-dichlorophenyl)-4-oxobutyl]-1-phenylpyrazoleHCID 18930277—
Reactant5-[(1RS,2RS)-1-Acetoxy-2-(3,4-dichlorophenyl)-4-(4-acetamido-4-phenylpiperidino)butyl]-1-phenylpyrazoleHCID 18930280—
Product5-[(1RS,2RS)-2-(3,4-Dichlorophenyl)-1-hydroxy-4-(4-acetamido-4-phenylpiperidino)butyl]-1-phenylpyrazoleHCID 18930310—

Reaction Steps

5-[(1RS,2RS)-1-Acetoxy-2-(3,4-dichlorophenyl)-4-(4-acetamido-4-phenylpiperidino)butyl]-1-phenylpyrazole. Using a procedure similar to that described in Example 7, except using 4-acetamido-4-phenylpiperidine as the amine component and 5-[(1RS,2RS)-1-acetoxy-2-(3,4-dichlorophenyl)-4-oxobutyl]-1-phenylpyrazole as the aldehyde component, the title compound was obtained as a white foam (65%; NMR: 7.58 (d,1), 7.48-7.21 (m,11), 7.09 (d,1), 6.81 (dd,1), 6.22 (d,1), 6.09 (d,1), 5.39 (s,1), 3.06 (m,1), 2.51 (m,2), 2.31 (m,2), 2.15-2.00 (m,7), 1.98 (s,3), 1.96 (s,3), 1.75 (m,1), 1.43 (m,1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739149
Source datasetuspto-grants-1998_04
ORD IDord-16cc68a54eba48d1b68c7b666275753d
Source noteuspto-grants-1998_04