Sodium borohydride → HCID 54346140, compound

HRID 328554Notes

Reaction equation

HRID 328554 reaction equation
[C@@H:1]1([N:10]2[CH2:17][CH2:16][C:14](=[O:15])[NH:13][C:11]2=[O:12])[O:7][C@H:6]([CH2:8][OH:9])[C@H:4]([OH:5])[C@@H:2]1[OH:3].[BH4-].[Na+]>>[OH:15][CH:14]1[CH2:16][CH2:17][N:10]([C@@H:1]2[O:7][C@H:6]([CH2:8][OH:9])[C@H:4]([OH:5])[C@@H:2]2[OH:3])[C:11](=[O:12])[NH:13]1

Participants

3

Reactant 2

HCID 4311764Sodium borohydrideHCID 22796915HCID 22796915, compound

Product 1

HCID 54346140HCID 54346140, compound

Procedure

In the manner given in Example 2C 1-β-D-lyxofuranosyl-dihydrouracil was reduced with sodium borohydride to give 4-hydroxy-1-β-D-lyxofuranosyl-tetrahydro-2(1H)-pyrimidinone.

Sources & evidence

ORD record
ord-7037e97bfd5444edbb2d52333e81d63c
Source dataset
uspto-grants-1977_04
Patent number
US04017606

Reaction notes

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