Calcium Hydroxide → HCID 131714312, compound

HRID 485599Notes

Reaction equation

HRID 485599 reaction equation
C([O:8][C:9](=[O:47])[C@@H:10]1[CH2:14][CH2:13][CH2:12][N:11]1[C:15](=[O:46])[C@@H:16]1[CH2:20][CH2:19][CH2:18][N:17]1[C:21](=[O:45])[C@H:22]([CH2:30][CH2:31][CH2:32][CH:33](C(OCC1C=CC=CC=1)=O)[NH2:34])[NH:23][P:24]([CH2:28][CH3:29])([CH2:26][CH3:27])=[O:25])C1C=CC=CC=1.[OH-].[Ca+2:49].[OH-]>CO.O.[C].[Pd]>[Ca+2:49].[CH2:26]([P:24]([NH:23][C@H:22]([C:21]([N:17]1[CH2:18][CH2:19][CH2:20][C@H:16]1[C:15]([N:11]1[CH2:12][CH2:13][CH2:14][C@H:10]1[C:9]([O-:47])=[O:8])=[O:46])=[O:45])[CH2:30][CH2:31][CH2:32][CH2:33][NH2:34])([CH2:28][CH3:29])=[O:25])[CH3:27].[CH2:26]([P:24]([NH:23][C@H:22]([C:21]([N:17]1[CH2:18][CH2:19][CH2:20][C@H:16]1[C:15]([N:11]1[CH2:12][CH2:13][CH2:14][C@H:10]1[C:9]([O-:47])=[O:8])=[O:46])=[O:45])[CH2:30][CH2:31][CH2:32][CH2:33][NH2:34])([CH2:28][CH3:29])=[O:25])[CH3:27]

Participants

6

Procedure

Diethylphosphoryl-ε-carbobenzoxy-L-lysyl-L-prolyl-L-proline benzyl ester (2.48 g, 3.5 mmole) was dissolved in methanol (25 ml), and calcium hydroxide (0.133 g) suspended in water (10 ml) was added thereto. The catalytic reduction reaction was carried out in the presence of 5% palladium-carbon as catalyst. The catalyst was removed by filtration and the solvent was distilled off under reduced pressure. The thus obtained milk-white and candy-like residue was dissolved in water. After removal of insoluble matter by filtration, the solution was freeze-dried to obtain diethylphosphoryl-L-lysyl-L-prolyl-L-proline calcium salt (1.54 g, yield: 87.8%).

Workup

  1. additionwas added
  2. customThe catalytic reduction reaction
  3. customThe catalyst was removed by filtration
  4. distillationthe solvent was distilled off under reduced pressure
  5. dissolutionThe thus obtained milk-white and candy-like residue was dissolved in water
  6. customAfter removal of insoluble matter
  7. filtrationby filtration
  8. customthe solution was freeze-dried

Sources & evidence

ORD record
ord-5ddd7b43f8434f9ab59da914e36f263b
Source dataset
uspto-grants-1985_08
Patent number
US04536395

Reaction notes

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