Potassium Iodide → HCID 21471809, compound

HRID 2294840Notes

Reaction equation

HRID 2294840 reaction equation
Cl[CH2:2][CH2:3][C:4]1[S:14][C:7]2[C:8](=[O:13])[NH:9][CH2:10][CH2:11][CH2:12][C:6]=2[CH:5]=1.Cl.[F:16][C:17]1[CH:31]=[CH:30][C:20]2[C:21]([CH:24]3[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]3)=[N:22][O:23][C:19]=2[CH:18]=1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CN(C)C=O.C1(C)C=CC=CC=1>[F:16][C:17]1[CH:31]=[CH:30][C:20]2[C:21]([CH:24]3[CH2:25][CH2:26][N:27]([CH2:2][CH2:3][C:4]4[S:14][C:7]5[C:8](=[O:13])[NH:9][CH2:10][CH2:11][CH2:12][C:6]=5[CH:5]=4)[CH2:28][CH2:29]3)=[N:22][O:23][C:19]=2[CH:18]=1

Participants

7

Conditions

Temperature
90 °C

Procedure

A mixture of 800 mg of 2-chloroethyl-4,5,6,7-tetrahydro-8H-thieno[2,3-c]azepin-8-one, 920 mg of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine hydrochloride, 1.45 g of potassium carbonate and 580 mg of potassium iodide in 10 ml of dimethylformamide and 10 ml of toluene was stirred at 90° C. for 22 hours and concentrated in vacuo. To the residue were added ethyl acetate and water, and separated. The ethyl acetate layer was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on a silica gel and recrystallized from ethyl acetate to give 0.65 g of 2-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-8H-thieno[2,3-c]azepin-8-one, m.p. 192°-194° C.

Workup

  1. concentrationconcentrated in vacuo
  2. additionTo the residue were added ethyl acetate and water
  3. customseparated
  4. washThe ethyl acetate layer was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography on a silica gel
  8. customrecrystallized from ethyl acetate

Sources & evidence

ORD record
ord-9d990a0568674070a183f3d29309839b
Source dataset
uspto-grants-1997_11
Patent number
US05691330

Reaction notes

Loading…