2-Fluorobenzoic acid → 3-Butyl-8-chloro-1-{4-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]butyl}-3,7-dihydro-1H-purine-2,6-dione

HRID 1097688Notes

Reaction equation

HRID 1097688 reaction equation
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH2:11]([N:15]1[C:23]2[N:22]=[C:21]([Cl:24])[NH:20][C:19]=2[C:18](=[O:25])[N:17]([CH2:26][CH2:27][CH2:28][CH2:29]/[C:30](=[N:33]/[H])/[NH:31]O)[C:16]1=[O:35])[CH2:12][CH2:13][CH3:14]>CS(C)=O>[CH2:11]([N:15]1[C:23]2[N:22]=[C:21]([Cl:24])[NH:20][C:19]=2[C:18](=[O:25])[N:17]([CH2:26][CH2:27][CH2:28][CH2:29][C:30]2[N:31]=[C:4]([C:3]3[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=3[F:1])[O:6][N:33]=2)[C:16]1=[O:35])[CH2:12][CH2:13][CH3:14]

Participants

4

Reactant 2

HCID 99352-Fluorobenzoic acidHCID 178506472HCID 178506472, compound

Product 1

HCID 593955013-Butyl-8-chloro-1-{4-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]butyl}-3,7-dihydro-1H-purine-2,6-dioneYield 29%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Conditions

Temperature
90 °C

Procedure

2-Fluorobenzoic acid (36 mg, 0.25 mmol) and CDl (45 mg, 0.28 mmol) were stirred in anhydrous DMSO (0.9 ml) at rt for 1 h. (1Z)-5-(3-Butyl-8-chloro-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)-N-hydroxypentanimidamide (100 mg, 0.28 mmol) was added and the mixture was stirred at 90° C. for 16 h. The mixture was purified by MDAP. The product fraction was combined and concentrated to give the title compound as a white solid (33 mg, 29%).

Workup

  1. additionwas added
  2. customThe mixture was purified by MDAP
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-fde56e0c44f44f71ac5276f017cd8541
Source dataset
uspto-grants-2012_03
Patent number
US08143264B2

Reaction notes

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