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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970411Generated: November 1, 2026

Benzaldehyde → HCID 23509675, compound

https://huagongshe.com/reaction/970411

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 numberUS07312222B2
Source datasetuspto-grants-2007_12
ORD IDord-3d89e6c9a7ca4b30a3847a2762a875eb
Source noteuspto-grants-2007_12