Sodium Iodide → HCID 9953176, compound

HRID 1057597Notes

Reaction equation

HRID 1057597 reaction equation
[CH2:1]([N:8]1[C:20]2[CH:19]=[CH:18][CH:17]=[C:16]([OH:21])[C:15]=2[C:14]2[C:9]1=[C:10]([Cl:22])[CH:11]=[CH:12][CH:13]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[CH2:24]([N:26]([CH2:30][CH3:31])[CH2:27][CH2:28]Cl)[CH3:25].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+]>CN(C=O)C>[CH2:1]([N:8]1[C:20]2[CH:19]=[CH:18][CH:17]=[C:16]([O:21][CH2:25][CH2:24][N:26]([CH2:30][CH3:31])[CH2:27][CH3:28])[C:15]=2[C:14]2[C:9]1=[C:10]([Cl:22])[CH:11]=[CH:12][CH:13]=2)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

9-Benzyl-8-chloro-9H-carbazol-4-ol (0.0826 g, 0.27mmol), 2-diethylaminoethylchloride hydrochloride (0.0719 g, 0.42 mmol), potassium carbonate (0.1157 g, 0.84 mmol), sodium iodide (0.0031 g, 0.021 mmol) and DMF (1 mL) are heated at 85° C. for 4 h. After the mixture had cooled, it is partitioned between water and ether. The combined organic layers are dried over magnesium sulfate and concentrated to an oil. The oil is chromatographed on silica gel (30 mL) using methanol/dichloromethane (1/99 to 2/98 to 4/96) to give 0.0675 g (62%) of the title compound: mp 73.5-75° C.; MS (ESI+) for C25H27ClN2O m/z 407.3 (M+H)+; IR (drift) 2966, 1588, 1499, 1454, 1413, 1355, 1337, 1266, 1124, 1027, 789, 732, 727, 717, 697 cm−1; 1H NMR (CDCl3) δ1.13, 2.72, 3.10, 4.33, 5.99, 6.71, 6.96, 7.10, 7.15-7.26, 7.33, 8.33. Anal. Calcd for C25H27ClN2O: C, 73.79; H, 6.69; N, 6.88. Found: C, 73.47; H, 6.81; N, 6.76.

Workup

  1. temperatureAfter the mixture had cooled
  2. customit is partitioned between water and ether
  3. dry with materialThe combined organic layers are dried over magnesium sulfate
  4. concentrationconcentrated to an oil
  5. customThe oil is chromatographed on silica gel (30 mL)

Sources & evidence

ORD record
ord-e3b9852bdd8f4aff91cb0281e57cf11d
Source dataset
uspto-grants-2003_02
Patent number
US06514968B1

Reaction notes

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