Sodium hydride → HCID 58515258, compound

HRID 1893391Notes

Reaction equation

HRID 1893391 reaction equation
[C:1]([N:8]1[CH2:12][CH2:11][CH:10]([OH:13])[CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[H-].[Na+].[Br:16][C:17]1[C:18](Cl)=[N:19][C:20]([Cl:23])=[N:21][CH:22]=1>C1COCC1>[Br:16][C:17]1[C:18]([O:13][CH:10]2[CH2:11][CH2:12][N:8]([C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])[CH2:9]2)=[N:19][C:20]([Cl:23])=[N:21][CH:22]=1

Participants

5

Procedure

To a solution of N-Boc-3-hydroxypyrrolidine (2.06 g, 11 mmol) in anhydrous THF (50 mL), was added NaH (60% oil dispersion, 0.44 g, 11 mmol). The mixture was stirred at room temperature for 19 h. The reaction mixture was cooled to −0° C. and was added slowly to a solution of 5-bromo-2,4-dichloropyrimidine (2.28 g, 10 mmol) in anhydrous THF (20 mL) at −5° C. The resulting mixture was stirred at −0° C. for 5 h and quenched with water. The aqueous solution was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo. The residue was purified on ISCO (hexane/ethyl acetate gradient, 0-20%) to give the title compound (3.0 g, 79.2%) as colorless oil. MS (ESI) m/z: Found: 378.0 (M++1); Calc. 377.0 (M+)

Workup

  1. temperatureThe reaction mixture was cooled to −0° C.
  2. stirringThe resulting mixture was stirred at −0° C. for 5 h
  3. customquenched with water
  4. extractionThe aqueous solution was extracted with ethyl acetate (3×50 mL)
  5. dry with materialThe combined organic layers were dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified on ISCO (hexane/ethyl acetate gradient, 0-20%)

Sources & evidence

ORD record
ord-bee036cc4e044305999e73341ea1df34
Source dataset
uspto-grants-2013_08
Patent number
US08513242B2

Reaction notes

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