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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270096Generated: October 31, 2026

Benzaldehyde → HCID 23509675, compound

https://huagongshe.com/reaction/2270096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 23509691HCID 23509691—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 23509675HCID 2350967519%

Reaction Steps

A solution of N-(3-cyanophenyl)-3-{[4-(4-fluorobenzyl)-1-piperidinyl]methyl}-1-piperazinecarboxamide dihydrochloride (20.0 mg, 0.05 mmol) and benzaldhyde (8.5 mg, 0.08 mmol, Aldrich) in dry dichloroethane (5 mL) was stirred for 20 min when sodium triacetoxyborohydride (32 mg, 0.15 mmol, Aldrich) was added. The reaction was stirred for 16 h and then quenched with water (5 mL). The organic layer was separated, dried over MgSO4, and conc. in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, EtOAc and then EtOAc:TEA, 9:1) to yield 5.0 mg of 4-benzyl-N-(3-cyanophenyl)-3-{[4-(4-fluorobenzyl)-1-piperidinyl]methyl}-1-piperazinecarboxamide as a white solid. MS (ESI) 526 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331545B1
Source datasetuspto-grants-2001_12
ORD IDord-e71832a1fc744fe4ae0d19e852e8dfdd
Source noteuspto-grants-2001_12