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635319-09-4

635319-09-4 Structure

635319-09-4 Structure
IdentificationBack Directory
[Name]

(3R,4R)-tert-Butyl 3-Hydroxy-4-(hydroxyMethyl)pyrrolidine-1-carboxylate
[CAS]

635319-09-4
[Synonyms]

(3R,4R)-tert-Butyl 3-Hydroxy-4-(hydroxyMethyl)pyrrolidine-1-carboxylate
tert-butyl (3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidine-1-carboxylate
1,1-Dimethylethyl (3R,4R)-3-hydroxy-4-(hydroxymethyl)-1-pyrrolidinecarboxylate
1-Pyrrolidinecarboxylic acid, 3-hydroxy-4-(hydroxymethyl)-, 1,1-dimethylethyl ester, (3R,4R)-
[Molecular Formula]

C10H19NO4
[MOL File]

635319-09-4.mol
[Molecular Weight]

217.26
Chemical PropertiesBack Directory
[Boiling point ]

340.3±27.0 °C(Predicted)
[density ]

1.190±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

14.49±0.40(Predicted)
[Appearance]

Light yellow to brown Solid
[Optical Rotation]

15°(C=0.01g/ml MEOH)
Hazard InformationBack Directory
[Uses]

(3R,4R)-tert-Butyl 3-Hydroxy-4-(hydroxymethyl)pyrrolidine-1-carboxylate has been used as a reactant for the preparation of transition state analogue inhibitors of human 5’-Methylthioadenosine phosphorylase (MTAP).
[Synthesis]

1-Pyrrolidinecarboxylic acid, 3-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-, 1,1-dimethylethyl ester, (3S,4R)-

635319-08-3

(3R,4R)-tert-Butyl 3-Hydroxy-4-(hydroxyMethyl)pyrrolidine-1-carboxylate

635319-09-4

The general procedure for the synthesis of tert-butyl (3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidine-1-carboxylate from the compound (CAS: 635319-08-3) was as follows: to an ethanol ((S)-1,2-dihydroxyethyl)pyrrolidine (3.4 g, 13.7 mmol) solution of N-tert-butoxycarbonyl-(3R,4S)-3-hydroxy-4-[(S)-1,2-dihydroxyethyl]pyrrolidine ( 50 mL) solution of sodium periodate (3.4 g, 16 mmol) was added dropwise to an aqueous (25 mL) solution of sodium periodate (3.4 g, 16 mmol) while maintaining the reaction temperature at 0 °C. The reaction mixture was continued to be stirred at 0 °C for 20 min. Subsequently, sodium borohydride (2.0 g, excess) was added in batches to ensure that the reaction temperature was maintained at 0 °C. After completion of addition, the solids were removed by filtration and the filter cake was washed with ethanol (50 mL). The filtrates were combined and concentrated in vacuum to give a syrupy product. Purification by column chromatography gave the target product 1 (2.74 g, 92% yield) in syrupy form.

[References]

[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 24, p. 5271 - 5276
[2] Patent: WO2004/18496, 2004, A1. Location in patent: Page 23-24
Spectrum DetailBack Directory
[Spectrum Detail]

(3R,4R)-tert-Butyl 3-Hydroxy-4-(hydroxyMethyl)pyrrolidine-1-carboxylate(635319-09-4)1HNMR
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