HCID 15896003, compound → HCID 445018, compound

HRID 2184783Notes

Reaction equation

HRID 2184783 reaction equation
C([O:8][NH:9][C:10]([C@H:12]1[CH2:17][C:16](=[O:18])[N:15]([CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:14][N:13]1[S:26]([C:29]1[CH:34]=[CH:33][C:32]([O:35][CH3:36])=[CH:31][CH:30]=1)(=[O:28])=[O:27])=[O:11])C1C=CC=CC=1>CO.[Pd]>[OH:8][NH:9][C:10]([C@H:12]1[CH2:17][C:16](=[O:18])[N:15]([CH2:19][C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH2:14][N:13]1[S:26]([C:29]1[CH:30]=[CH:31][C:32]([O:35][CH3:36])=[CH:33][CH:34]=1)(=[O:28])=[O:27])=[O:11]

Participants

4

Procedure

A mixture of N-benzyloxy 1-benzyl-3-[(4-Methoxyphenyl)sulfonyl]-6-oxo-hexahydro-pyrimidine-4(R)carboxamide (213 mg, 0.4 mmol) and 10% Pd/C (50 mg) in methanol (25 mL) is stirred under hydrogen atmosphere for 3 hours. The mixture is filtered over celite and the filtrate is collected and concentrated under reduced pressure to give an oil. The crude product is purified by flash silica gel chromatography (200:1 ethyl acetate-formic acid) to give N-hydroxy 1-benzyl-3-[(4-methoxyphenyl)sulfonyl]-6-oxo-hexahydro-pyrimidine-4(R)carboxamide as a white solid. MS (ESI): 420 (M+H+), 437 (M+NH4+).

Workup

  1. filtrationThe mixture is filtered over celite
  2. customthe filtrate is collected
  3. concentrationconcentrated under reduced pressure
  4. customto give an oil
  5. customThe crude product is purified by flash silica gel chromatography (200:1 ethyl acetate-formic acid)

Sources & evidence

ORD record
ord-fa2864672e1f46538c9ff019f9b7c70e
Source dataset
uspto-grants-2002_06
Patent number
US06399598B1

Reaction notes

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