Potassium Iodide → HCID 15124793, compound

HRID 486433Notes

Reaction equation

HRID 486433 reaction equation
Cl[CH2:2][CH2:3][N:4]([CH2:15][CH2:16][CH2:17]Cl)[S:5]([C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=1)(=[O:7])=[O:6].[CH3:19][C:20]1[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][C:21]=1[NH2:27].C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+].C1(O)CCCCC1>O>[CH3:19][C:20]1[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][C:21]=1[N:27]1[CH2:17][CH2:16][CH2:15][N:4]([S:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)(=[O:7])=[O:6])[CH2:3][CH2:2]1

Participants

7

Procedure

A mixture of 93 parts of N-(2-chloroethyl)-N-(3-chloropropyl)-4-methylbenzenesulfonamide, 30.3 parts of 2,3-dimethylbenzenamine, 63.6 parts of sodium carbonate, 1 part of potassium iodide and 240 parts of cyclohexanol was stirred and refluxed over weekend using a water separator. After cooling, the reaction mixture was poured into water. The product was extracted with methylbenzene. The extract was washed twice with water, dried, filtered and evaporated. The residue was crystallized from 2-propanol and a small amount of tetrahydrofuran. The product was filtered off and dried, yielding 47.8 parts (53.3%) of 1-(2.3-dimethylphenyl)hexahydro-4-[(4-methylphenyl)sulfonyl]-1H-1.4-diazepine; mp. 86.2° C. (intermediate 7).

Workup

  1. temperaturerefluxed over weekend
  2. temperatureAfter cooling
  3. extractionThe product was extracted with methylbenzene
  4. washThe extract was washed twice with water
  5. customdried
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was crystallized from 2-propanol
  9. filtrationThe product was filtered off
  10. customdried

Sources & evidence

ORD record
ord-45a65385eb624b159aedfbbe7b5360c5
Source dataset
uspto-grants-1994_03
Patent number
US05292738

Reaction notes

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