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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276509Generated: November 1, 2026

Ammonium formate → 3-(SR)-(4-(2-tolyl)-piperidin-1-ylmethyl)-4-(SR)-phenylpyrrolidine

https://huagongshe.com/reaction/1276509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Benzyl-3-(SR)-(4-(2-tolyl)-piperidin-1-ylmethyl)-4-(SR)-phenylpyrrolidineHCID 70199440—
CatalystPalladiumHCID 23938—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product3-(SR)-(4-(2-tolyl)-piperidin-1-ylmethyl)-4-(SR)-phenylpyrrolidineHCID 70200483—

Reaction Steps

The title compound was prepared from 15 mg of 1-Benzyl-3-(SR)-(4-(2-tolyl)-piperidin-1-ylmethyl)-4-(SR)-phenylpyrrolidine (from Example 20), 35 mg of ammonium formate and 8 mg of 10% Pd on carbon in 1.5 mL of MeOH using a procedure analogous to that described in Example 30, Step A (except Pd on carbon was substituted for 20% Pd(OH)2) to provide the title compound, which was taken onto Step B without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166037
Source datasetuspto-grants-2000_12
ORD IDord-d405090328464c60b3efe8a7c71cacd6
Source noteuspto-grants-2000_12