Bromine → HCID 15838748, compound

HRID 619302Notes

Reaction equation

HRID 619302 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]([F:18])=[CH:10][CH:9]=2)[CH:5]=[C:4]([CH:19]([CH3:21])[CH3:20])[N:3]=1.[Br:22]Br.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)(Cl)Cl.[Fe]>[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]([F:18])=[CH:10][CH:9]=2)[C:5]([Br:22])=[C:4]([CH:19]([CH3:21])[CH3:20])[N:3]=1

Participants

6

Procedure

To a solution of 2-amino-4-(4-fluoronaphth-1-yl)-6-isopropyl-pyrimidine (free base, 0.100 g) in carbon tetrachloride (10 mL) was added iron powder (0.002 g) and bromine (0.074 g) at room temperature. The reaction mixture was stirred at room temperature for 1 hour, after which time it was poured into sodium bicarbonate solution (saturated, 30 mL). The layers were separated and the aqueous layer was extracted three times with methylene chloride (3×10 mL). The combined organic layers were evaporated to dryness. The residue was purified by preparative thin layer chromatography, eluting with hexane/ethyl acetate, and recrystallized from ether/hexane to give 2-amino-5-bromo-4-(4-fluoronaphth-1-yl)-6-isopropyl-pyrimidine (0.072 g), m.p. 176-180° C.

Workup

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted three times with methylene chloride (3×10 mL)
  3. customThe combined organic layers were evaporated to dryness
  4. customThe residue was purified by preparative thin layer chromatography
  5. washeluting with hexane/ethyl acetate
  6. customrecrystallized from ether/hexane

Sources & evidence

ORD record
ord-37a0176ccfb042bc8e328e6a72f0963e
Source dataset
uspto-grants-1999_09
Patent number
US05958934

Reaction notes

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