Methanol → HCID 22648007, compound

HRID 394171Notes

Reaction equation

HRID 394171 reaction equation
[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[C:11]([O:15][C:16](=[O:18])[CH3:17])([CH3:14])([CH3:13])[CH3:12].Br[CH2:20][C:21]1[C:22]([Cl:37])=[N:23][C:24]([S:35][CH3:36])=[N:25][C:26]=1[C:27]1[CH:32]=[CH:31][C:30]([F:33])=[CH:29][C:28]=1[F:34].CO>C1COCC1>[Cl:37][C:22]1[C:21]([CH2:20][CH2:17][C:16]([O:15][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:18])=[C:26]([C:27]2[CH:32]=[CH:31][C:30]([F:33])=[CH:29][C:28]=2[F:34])[N:25]=[C:24]([S:35][CH3:36])[N:23]=1

Participants

6

Reactant 4

HCID 887MethanolHCID 10908tert-Butyl acetateHCID 2733832Lithium HexamethyldisilazideHCID 22648121HCID 22648121, compound

Product 1

HCID 22648007HCID 22648007, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-50 °C

Procedure

To a −78° C. solution of LiHMDS (4.1 mL) in 3 mL of THF was added t-butylacetate (0.6 mL). After stirring for 10 min, 1.0 g of 5-(bromomethyl)-4-chloro-6-(2,4-difluorophenyl)-2-(methylthio)pyrimidine (COMPOUND VV-3) in 4 mL of THF was added dropwise. The mixture was stirred at −78° C. for 1.5 h, then warmed to −50° C. The reaction mixture was recooled to −78° C. and 3 mL of methanol was added. The solution stirred for 24 h at rt. The crude mixture was purified by flash chromatography, eluting with 2% diethyl ether/hexanes. Mass spectrum m/z (ESI) 401.5 (M+1).

Workup

  1. stirringThe mixture was stirred at −78° C. for 1.5 h
  2. customwas recooled to −78° C.
  3. stirringThe solution stirred for 24 h at rt
  4. customThe crude mixture was purified by flash chromatography
  5. washeluting with 2% diethyl ether/hexanes

Sources & evidence

ORD record
ord-385412c2a46044e5bf6ee848c1615286
Source dataset
uspto-grants-2004_10
Patent number
US06809199B2

Reaction notes

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