HCID 86747727, compound → HCID 6923529, compound

HRID 1463302Notes

Reaction equation

HRID 1463302 reaction equation
C[C@@H](OC([N:12]1[C@@H:16]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C@H:15]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:14](=[O:29])[NH:13]1)=O)C1C=CC=CC=1>[Pd].C1COCC1>[C:23]1([C@H:15]2[C@H:16]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[NH:12][NH:13][C:14]2=[O:29])[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

Participants

4

Reactant 1

HCID 86747727HCID 86747727, compound

Product 1

HCID 6923529HCID 6923529, compoundYield 96%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 8028TetrahydrofuranSolvent

Procedure

A thick-walled glass hydrogenation tube was charged with diastereomer B of 1-[((R)-α-methylbenzyl)oxycarbonyl]-trans-4,5-diphenyl-3-pyrazol idinone [from Example 139A/139B] (226 mg, 0.586 mmol), 15.0 mL THF and 5% Pd/C catalyst (112 mg) and was shaken on a Parr apparatus under an atmosphere of hydrogen at c. 50 psi pressure for 15.5 hr. The catalyst was filtered off using Celite and washed with THF. The filtrate was evaporated in vacuo to obtain 134 mg (96%) of a white foam:

Workup

  1. filtrationThe catalyst was filtered off
  2. washwashed with THF
  3. customThe filtrate was evaporated in vacuo

Sources & evidence

ORD record
ord-b8964fd5d450405c9c5956597576d46a
Source dataset
uspto-grants-1994_04
Patent number
US05300514

Reaction notes

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