4-(3-phenylpropyl)piperidin-4-ol

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 1-Benzyl-3-(R)-formyl-4-(S)-(3-thienyl)pyrrolidine [which was prepared from (S)-N-(1-benzyl-4-(S)-(3-thienyl)-3-(R)-pyrrolidinylcarbonyl)-4-benzyl-2-oxazolidinone (Example 241 Step 2)] and 4-hydroxy-4-(3-phenylpropyl)piperidine (Example 122, Step 1) by procedures analogous to those described in Example 241.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 1-benzyl-3-(SR)-formyl-4-(SR)-thiophen-3-ylpyrrolidine and 4-hydroxy-4-(3-phenylpropyl)piperidine by procedures described in Example 1.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 3.3 g (10.7 mmol) of 1-benzyl-4-hydroxy-4-(3-phenylpropyl)piperidine and 0.5 g of Pd(OH)2 (Pearlman's catalyst) in 80 mL of MeOH was hydrogenated at 50 psi for 24 h. The reaction mixture was filtered through a thin pad of celite and concentrated to give the title compound. The reaction mixture was filtered through a thin pad of celite concentrated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 1-Benzyl-3-(R)-formyl-4-(S)-(3-thienyl)pyrrolidine [which was prepared from (S)-N-(1-benzyl-4-(S)-(3-thienyl)-3-(R)-pyrrolidinylcarbonyl)-4-benzyl-2-oxazolidinone (Example 241 Step 2)] and 4-hydroxy-4-(3-phenylpropyl)piperidine (Example 122, Step 1) by procedures analogous to those described in Example 241.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 1-Benzyl-3-(R)-formyl-4-(S)-(3-thienyl)pyrrolidine [which was prepared from (S)-N-(1-benzyl-4-(S)-(3-thienyl)-3-(R)-pyrrolidinylcarbonyl)-4-benzyl-2-oxazolidinone (Example 241 Step 2)] and 4-hydroxy-4-(3-phenylpropyl)piperidine (Example 122, Step 1) by procedures analogous to those described in Example 241.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound was prepared from 1-benzyl-3-(SR)-formyl-4-(SR)-thiophen-3-ylpyrrolidine and 4-hydroxy-4-(3-phenylpropyl)piperidine by procedures described in Example 1.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 3.3 g (10.7 mmol) of 1-benzyl-4-hydroxy-4-(3-phenylpropyl)piperidine and 0.5 g of Pd(OH)2 (Pearlman's catalyst) in 80 mL of MeOH was hydrogenated at 50 psi for 24 h. The reaction mixture was filtered through a thin pad of celite and concentrated to give the title compound. The reaction mixture was filtered through a thin pad of celite concentrated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 3.3 g (10.7 mmol) of 1-benzyl-4-hydroxy-4-(3-phenylpropyl)piperidine and 0.5 g of Pd(OH)2 (Pearlman's catalyst) in 80 mL of MeOH was hydrogenated at 50 psi for 24 h. The reaction mixture was filtered through a thin pad of celite and concentrated to give the title compound. The reaction mixture was filtered through a thin pad of celite concentrated

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir: