Phosphorus oxychloride → HCID 86595016, compound

HRID 1792258Notes

Reaction equation

HRID 1792258 reaction equation
[CH3:1][C:2]1[N:3]=[C:4](O)[C:5]2[N:13]3[C:8]([C:9]([C:14]4[C:19]([CH3:20])=[CH:18][C:17]([CH3:21])=[CH:16][C:15]=4[CH3:22])=[CH:10][CH:11]=[CH:12]3)=[CH:7][C:6]=2[N:23]=1.P(Cl)(Cl)([Cl:27])=O>>[Cl:27][C:4]1[C:5]2[N:13]3[C:8]([C:9]([C:14]4[C:15]([CH3:22])=[CH:16][C:17]([CH3:21])=[CH:18][C:19]=4[CH3:20])=[CH:10][CH:11]=[CH:12]3)=[CH:7][C:6]=2[N:23]=[C:2]([CH3:1])[N:3]=1

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178424532HCID 178424532, compound

Product 1

HCID 86595016HCID 86595016, compound

Procedure

Heat at 100° C. for 2 h a solution of 2-methyl-9-(2,4,6-trimethylphenyl)pyrimidino[4,5-b]indolizin-4-ol (120 mg) in phosphorus oxychloride (2 mL), cool to ambient temperature, and concentrate in vacuo. Partition the residue into ice water and CH2Cl2. Extract the aqueous phase twice with CH2Cl2 and wash the combined organic extracts with a saturated NaHCO3 solution. Dry the solution over Na2SO4, filter, and concentrate in vacuo. Purify the dark residue by column chromatography on silica gel (eluent: 10% to 20% EtOAc in hexane) to obtain the title compound as a greenish yellow foam: 1H NMR (400 MHz, CDCl3) δ 1.99 (s, 6H), 2.38 (s, 3H), 2.79 (s, 3H), 6.80 (m, 1H), 7.00 (s, 2H), 7.19 (m, 2H), 9.27 (d, 1H).

Workup

  1. concentrationconcentrate in vacuo
  2. customPartition the residue into ice water and CH2Cl2
  3. extractionExtract the aqueous phase twice with CH2Cl2
  4. washwash the combined organic extracts with a saturated NaHCO3 solution
  5. dry with materialDry the solution over Na2SO4
  6. filtrationfilter
  7. concentrationconcentrate in vacuo
  8. customPurify the dark residue by column chromatography on silica gel (eluent: 10% to 20% EtOAc in hexane)

Sources & evidence

ORD record
ord-4395eea2939440faae29dd616f8797af
Source dataset
uspto-grants-2006_07
Patent number
US07074929B2

Reaction notes

Loading…