HCID 178477759, compound → HCID 178511303, compound

HRID 856892Notes

Reaction equation

HRID 856892 reaction equation
[CH2-:1][C:2]([CH3:4])=[O:3].[N:5]([CH2:8][C@@H:9]1[C@H:13]([OH:14])[C@H:12]([OH:15])[C@H:11]([N:16]2[CH:24]=[N:23][C:22]3[C:17]2=[N:18][CH:19]=[N:20][C:21]=3[CH:25]2[CH2:29][CH2:28][O:27][CH2:26]2)[O:10]1)=[N+]=[N-]>C(O)C.[Pd]>[CH2-:1][C:2]([CH3:4])=[O:3].[NH2:5][CH2:8][C@@H:9]1[C@H:13]([OH:14])[C@H:12]([OH:15])[C@H:11]([N:16]2[CH:24]=[N:23][C:22]3[C:17]2=[N:18][CH:19]=[N:20][C:21]=3[CH:25]2[CH2:29][CH2:28][O:27][CH2:26]2)[O:10]1

Participants

4

Procedure

10%Pd/C (100 mg) was added to a solution of (4S,2R,3R,5R)-2-azidomethyl-5-[6-(tetrahydrofuran-3-yl)-purin-9-yl]-tetrahydrofuran-3,4-diol acetonide, a compound of formula (10) (314 mg), in ethanol (20 mL) and stirred under an atmosphere of hydrogen at room temperature for 16 hours. The catalyst was removed by filtration, and the solvent evaporated from the filtrate to give (4S,2R,3R,5R)-2-aminomethyl-5-[6-(tetrahydrofuran-3-yl)-purin-9-yl]-tetrahydrofuran-3,4-diol acetonide, a compound of formula (11).

Workup

  1. customThe catalyst was removed by filtration
  2. customthe solvent evaporated from the filtrate

Sources & evidence

ORD record
ord-6b06dc8e2d87484e8678c3cebe83a0a8
Source dataset
uspto-grants-2006_12
Patent number
US07144871B2

Reaction notes

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