Sulfur → HCID 59968960, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:34])[CH2:4][C@H:5]([NH:12][C:13](=[O:33])[CH2:14][NH:15][C:16](=[O:32])[CH2:17][CH2:18][CH2:19][CH2:20][NH:21][C:22]([NH:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[NH2:31])=S)[C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1.[S]>C(O)C>[CH3:1][O:2][C:3](=[O:34])[CH2:4][C@H:5]([NH:12][C:13](=[O:33])[CH2:14][NH:15][C:16](=[O:32])[CH2:17][CH2:18][CH2:19][CH2:20][NH:21][C:22]1[NH:31][C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=2[N:24]=1)[C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
An ethanol mixture(20 ml) of 24-7 (89 mg, 0.18 mmol), mercuric oxide (78.8 mg, 0.36 mmol) and sulfur (1.8 mg, 0.056 mmol) was refluxed for 2 hr. After cooling, the mixture was filtered and the filtrate concentrated to a semi-solid which was purified by flash chromatography (20% MeOH/CH2Cl2) to provide 24-8 as a solid.
Workup
- temperatureAfter cooling
- filtrationthe mixture was filtered
- concentrationthe filtrate concentrated to a semi-solid which
- customwas purified by flash chromatography (20% MeOH/CH2Cl2)
Sources & evidence
- ORD record
- ord-bc76c41369d14b57a06af620a0a01534
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05952306
Reaction notes
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