Carbon Dioxide → HCID 178515905, compound

HRID 1722013Notes

Reaction equation

HRID 1722013 reaction equation
[O:1]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]2[N:9]=[C:10]([C:13]3[CH:18]=[CH:17][C:16]([O:19]C)=[CH:15][CH:14]=3)[NH:11][CH:12]=2)[CH2:3][CH2:2]1.C(=O)=O.B(Br)(Br)Br.CO>C(Cl)Cl>[O:1]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]2[N:9]=[C:10]([C:13]3[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=3)[NH:11][CH:12]=2)[CH2:3][CH2:2]1

Participants

6

Procedure

Under N2, a solution of 52 (2.25 g, .0082 mol) in CH2Cl2 (25 ml) was added dropwise to a dry-ice cooled solution of BBr3 (2.5 ml, d=2.65, 0.0265 mol) in CH2C12 (75 ml). After the addition, the solution was stirred at room temperature overnight and then treated dropwise with CH3OH (50 ml). After stirring overnight at room temperature, the solution was concentrated to dryness, the residue treated with 10% NaOH, the aqueous layer extracted with Et2O, the pH of the solution adjusted to 8.7 and concentrated to dryness. The residue was triturated with hot CH3OH, filtered, the filtrate concentrated to dryness and the residue chromatographed on silica gel. The product was eluted with 10% CH3OH-CHCl3 to yield 1.75 g (82%) of 53.

Workup

  1. additionAfter the addition
  2. stirringAfter stirring overnight at room temperature
  3. concentrationthe solution was concentrated to dryness
  4. additionthe residue treated with 10% NaOH
  5. extractionthe aqueous layer extracted with Et2O
  6. concentrationconcentrated to dryness
  7. customThe residue was triturated with hot CH3OH
  8. filtrationfiltered
  9. concentrationthe filtrate concentrated to dryness
  10. customthe residue chromatographed on silica gel
  11. washThe product was eluted with 10% CH3OH-CHCl3

Sources & evidence

ORD record
ord-c4aa123c5c33492fa49db2b205ec3222
Source dataset
uspto-grants-1989_08
Patent number
US04853383

Reaction notes

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