Tetrahydrofuran → (R)-7-chloro-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridine

HRID 2357968Notes

Reaction equation

HRID 2357968 reaction equation
[Cl:1][C:2]1[N:11]=[CH:10][C:9]2[NH:8][C:7](=O)[C@@H](CC)[N:5]([CH:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)[C:4]=2[N:3]=1.[NH2:20][NH2:21].[CH2:22]1[CH2:26]O[CH2:24][CH2:23]1.C(OCC)(=O)C>P(Cl)(Cl)(Cl)=O>[Cl:1][C:2]1[N:11]=[CH:10][C:9]2[N:8]3[CH:7]=[N:20][N:21]=[C:24]3[C@@H:23]([CH2:22][CH3:26])[N:5]([CH:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)[C:4]=2[N:3]=1

Participants

6

Reactant 4

HCID 8028TetrahydrofuranHCID 8857Ethyl AcetateHCID 9321HydrazineHCID 24739252(R)-2-chloro-8-cyclopentyl-7-ethyl-7,8-dihydropteridin-6(5H)-one

Product 1

HCID 59389586(R)-7-chloro-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridineYield 63%

Reagents, catalysts & solvents 1

HCID 24813Phosphorus oxychlorideSolvent

Procedure

(R)-2-Chloro-8-cyclopentyl-7-ethyl-7,8-dihydropteridin-6(5H)-one (100 mg, 0.357 mmol) in phosphorus oxychloride (3.0 ml) was stirred at 110° C. for 3 hours then concentrated under reduced pressure. The residue was dissolved in anhydrous dichloromethane and added dropwise to 1.0 M hydrazine in THF (3.6 ml, 3.57 mmol). The mixture was stirred at RT overnight, taken into ethyl acetate and washed with aqueous sodium hydrogen carbonate, dried over magnesium sulphate and concentrated. The residue of crude hydrazide was dissolved in trimethyl orthoformate (2.0 ml) and stirred at 110° C. for 90 min. The mixture was concentrated under reduced pressure and purified by flash chromatography on silica gel eluting with ethyl acetate to give (R)-7-chloro-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridine (68 mg, 63%) as a pale brown solid; 1H NMR (DMSO D6) 0.75 (3H, t), 1.50-1.64 (2H, m), 1.80-2.08 (8H, m), 4.22-4.33 (1H, m), 5.28-5.35 (1H, m), 8.68 (1H, s), 9.35 (1H, s); MS (ES+) 305.

Workup

  1. concentrationthen concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in anhydrous dichloromethane
  3. washwashed with aqueous sodium hydrogen carbonate
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated
  6. dissolutionThe residue of crude hydrazide was dissolved in trimethyl orthoformate (2.0 ml)
  7. stirringstirred at 110° C. for 90 min
  8. concentrationThe mixture was concentrated under reduced pressure
  9. custompurified by flash chromatography on silica gel eluting with ethyl acetate

Sources & evidence

ORD record
ord-8d0d66b27d694219b4c0bab1042aa09d
Source dataset
uspto-grants-2010_07
Patent number
US07763629B2

Reaction notes

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