HCID 69040327, compound → HCID 69039807, compound

HRID 1454241Notes

Reaction equation

HRID 1454241 reaction equation
C(OC(=O)[NH:10][CH:11]1[CH2:30][CH2:29][CH2:28][CH2:27][C:12]21[CH2:17][N:16]([CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=1)[CH2:15][CH2:14][CH2:13]2)C1C=CC=CC=1>CO.[Pd]>[F:26][C:23]1[CH:24]=[CH:25][C:20]([CH2:19][CH2:18][N:16]2[CH2:15][CH2:14][CH2:13][C:12]3([CH2:27][CH2:28][CH2:29][CH2:30][CH:11]3[NH2:10])[CH2:17]2)=[CH:21][CH:22]=1

Participants

4

Procedure

A solution of {2-[2-(4-fluoro-phenyl)-ethyl]-2-aza-spiro[5.5]undec-7-yl}-carbamic acid benzyl ester (0.60 g, 1.4 mmol) in methanol (30 mL) was treated with 10% palladium on carbon (1.0 g) and shaken under a hydrogen atmosphere (60 psig) for 20 hours at room temperature. The catalyst was removed by filtration and the solvent was removed under vacuum to give a white foam (0.35 g).

Workup

  1. customThe catalyst was removed by filtration
  2. customthe solvent was removed under vacuum

Sources & evidence

ORD record
ord-b5c4da35dea8474a97c7e158418a939c
Source dataset
uspto-grants-2009_01
Patent number
US07479496B2

Reaction notes

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