Methyl chloroformate → HCID 24890786, compound

HRID 2357976Notes

Reaction equation

HRID 2357976 reaction equation
[CH:1]1([N:6]2[C:15]3[N:14]=[C:13]([NH2:16])[N:12]=[CH:11][C:10]=3[N:9]3[CH:17]=[N:18][N:19]=[C:8]3[C@H:7]2[CH2:20][CH3:21])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Na+].ClC(OC)=O.[Cl-].[NH4+:30]>CN(C=O)C>[CH:1]1([N:6]2[C:15]3[N:14]=[C:13]([NH:16][C:2]4[CH:3]=[N:30][CH:4]=[CH:5][CH:1]=4)[N:12]=[CH:11][C:10]=3[N:9]3[CH:17]=[N:18][N:19]=[C:8]3[C@H:7]2[CH2:20][CH3:21])[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

6

Reactant 4

HCID 6586Methyl chloroformateHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 24890788HCID 24890788, compound

Product 1

HCID 24890786HCID 24890786, compoundYield 31%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To (R)-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridin-7-amine (50 mg, 0.175 mmol) in DMF (1 ml) at 0° C. was added sodium hydride (60% in mineral oil, 7.7 mg, 0.193 mmol). The reaction mixture was stirred for 10 minutes, then methyl chloroformate (13.6 μL, 0.175 mmol) was added. The reaction was allowed to warm up to room temperature and was stirred for 18 hours. Ammonium chloride (5 ml, sat. aq. soln.) was added and extracted with EtOAc (3×10 ml). The combined organics were washed with brine (10 ml), dried over MgSO4, filtered and the solvent removed under vacuum. The crude product was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 □M, 100 Å column, gradient 10%-95% B (solvent A: 0.05% TFA in water; solvent B: CH3CN) over 16 minutes at 25 mL/min] to afford the title compound as an off-white powder (25 mg, 31%).

Workup

  1. stirringwas stirred for 18 hours
  2. extractionextracted with EtOAc (3×10 ml)
  3. washThe combined organics were washed with brine (10 ml)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customthe solvent removed under vacuum
  7. customThe crude product was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 □M, 100 Å column, gradient 10%-95% B (solvent A: 0.05% TFA in water; solvent B: CH3CN) over 16 minutes at 25 mL/min]

Sources & evidence

ORD record
ord-a995e108e89f4e35853167241e2e8b67
Source dataset
uspto-grants-2010_07
Patent number
US07763629B2

Reaction notes

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