Lithium → 2-(Tetrahydro-6-hydroxy-2,2dimethylfuro[2,3-d]-l,3-dioxol-5-yl)-3-pyrrolidinol
Reaction equation
[OH:1][CH:2]1[CH:6]([CH:7]2[O:16][CH:10]3[O:11][C:12]([CH3:15])([CH3:14])[O:13][CH:9]3[CH:8]2[OH:17])[NH:5][C:4](=O)[CH2:3]1.[Li]>>[OH:17][CH:8]1[CH:9]2[CH:10]([O:11][C:12]([CH3:15])([CH3:14])[O:13]2)[O:16][CH:7]1[CH:6]1[CH:2]([OH:1])[CH2:3][CH2:4][NH:5]1Participants
Procedure
A process according to claim 1 for converting 5-(t-BOC)amino -5-deoxy-l,2-0-isopropylidene-α-D-glucuronolactone to castanospermine which comprises (a) reacting 5-(t? -0 BOC)amino-5-deoxy-l,2-O-isopropylidene-α-D-glucuronolactone (I) with ethyl acetate and lithium diisopropylamine in an inert solvent at low temperature whereby the ethyl acetate adds across the carbonyl group of the lactone to give the corresponding cyclic hemiketal of an β-keto ester (II); (b) hydrogenating the hemiketal catalytically under pressure over a platinum oxide catalyst in ethyl acetate to reduce the β-keto function and give β-hydroxy ester (III); (c) treating the β-hydroxy ester with formic acid in an inert solvent with cooling to remove the protecting group from the amine followed by basification of the resulting amine salt using a basic ion exchange resin to provide internal cyclization of the amine to give lactam (IV); (d) reducing the lactam with lithium aluminumhydride to give the corresponding pyrrolidine (V); and (e) treating the pyrrolidine first with trifluoroacetic acid with cooling and then hydrogenating over platinum or carbon catalyst under pressure to give castanospermine (VI).
Sources & evidence
- ORD record
- ord-0a6a22cf4a5c4e5b9a8adbaff79ee288
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05066807
Reaction notes
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