反応式
C(OC([N:11]1[CH2:19][C@@H:18]([OH:20])[CH2:17][C@H:12]1[C:13]([O:15][CH3:16])=[O:14])=O)C1C=CC=CC=1.[ClH:21]>[Pd].CO>[ClH:21].[OH:20][C@@H:18]1[CH2:19][NH:11][C@H:12]([C:13]([O:15][CH3:16])=[O:14])[CH2:17]1参加物
実験手順
Into a 1 liter Parr hydrogenation bottle was placed 29.90 g (107.12 mmol) of (cis)-1-benzyloxycarbonyl-4-hydroxy-L-proline, methyl ester (reference: J. Am. Chem. Soc., 79, 185, (1957)), 400 ml of methanol, 9.83 ml (117.90 mmol) of concentrated HCl, and 3.00 g of 10% palladium on activated carbon. The mixture was shaken under a hydrogen atmosphere at 50 psi for 4 hours, then filtered through a Millipore filter; the palladium was washed with 100 ml of methanol. The filtrate was concentrated under vacuum to a minimal volume, then treated with 250 ml of ethyl acetate, which caused a white precipitate to form. The solids were filtered, washed twice with ethyl acetate and once with hexane, and dried under vacuum to yield 20.05 g (93.1%) of the title compound.
後処理
- filtrationfiltered through a Millipore
- filtrationfilter
- washthe palladium was washed with 100 ml of methanol
- concentrationThe filtrate was concentrated under vacuum to a minimal volume
- additiontreated with 250 ml of ethyl acetate, which
- customto form
- filtrationThe solids were filtered
- washwashed twice with ethyl acetate and once with hexane
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-275a00f4136c4a85acaea719e14a257b
- 出典データセット
- uspto-grants-1990_03
- 特許番号
- US04912231
関連ノート
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