Hydrochloric Acid → HCID 70981527, compound

HRID 879257Notes

Reaction equation

HRID 879257 reaction equation
[Br:1][C:2]1[S:3][C:4]2[C:10](=[O:11])[CH2:9][CH:8]([CH3:12])[CH2:7][C:5]=2[N:6]=1.C1C(=O)N(Br)C(=O)C1.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.C1CCN2C(=NCCC2)CC1.Cl>C(Cl)(Cl)(Cl)Cl.C(Cl)Cl>[Br:1][C:2]1[S:3][C:4]2[C:10]([OH:11])=[CH:9][C:8]([CH3:12])=[CH:7][C:5]=2[N:6]=1

Participants

8

Conditions

Temperature
90 °C

Procedure

To a solution of 26 (7.38 g, 30.0 mmol) in CCl4 (90 mL) was added NBS (5.61 g, 31.5 mmol) and dibenzoyl peroxide (727 mg, 3.0 mmol). The reaction was heated at 90° C. in a sealed reaction vessel for about 4 h. Then DBU (6.73 mL, 45.0 mmol) in CH2Cl2 (15 mL) was added. The mixture was heated a reflux for 30 min, then a 1 M HCl solution was added. The layers were separated, and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with a brine solution. The organic layer was then dried, filtered, and concentrated in vacuo. The crude product was adsorbed on ˜30 g of silica then run through a plug of silica with 40% EtOAc/hexanes to give 5.2 g of 27. 1H-NMR: 400 MHz, (CD3OH) δ: 7.25 (s, 1H), 6.69 (s, 1H), 2.40 (s, 3H). LCMS-ESI+: calc'd for C8H7BrNOS: 243.9 (M+H+); Found: 244.1 (M+H+).

Workup

  1. temperatureThe mixture was heated
  2. temperaturea reflux for 30 min
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with CH2Cl2
  5. washThe combined organic layers were washed with a brine solution
  6. customThe organic layer was then dried
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-ff19afeb7a58449098a4988cdec91603
Source dataset
uspto-grants-2015_03
Patent number
US08987250B2

Reaction notes

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