Chlorosuccinimide → HCID 14232132, compound

HRID 1613951Notes

Reaction equation

HRID 1613951 reaction equation
[CH2:1]([O:3][C:4](=[O:17])[N:5]([C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1)[N:6]1[CH:10]=[CH:9][CH:8]=[CH:7]1)[CH3:2].[Cl:18]N1C(=O)CCC1=O.S(=O)(O)[O-].[Na+]>O1CCCC1>[ClH:18].[CH2:1]([O:3][C:4](=[O:17])[N:5]([N:6]1[CH:10]=[CH:9][CH:8]=[C:7]1[Cl:18])[C:11]1[CH:12]=[CH:13][N:14]=[CH:15][CH:16]=1)[CH3:2]

Participants

5

Procedure

To a solution of N-(4-pyridinyl)-N-(1H-pyrrol-1-yl) carbamic acid ethyl ester (9 g) in 100 ml of anhydrous tetrahydrofuran warmed to 50o was slowly dropped a solution of N-chlorosuccinimide (5.2 g) in 75 ml of anhydrous tetrahydrofuran. After stirring seven hours at 50°, the reaction mixture was cooled, stirred with an aqueous solution of sodium bisulfite and extracted with ethyl acetate. The organic extract was washed with water and saturated sodium chloride and thereafter dried over anhydrous magnesium sulfate, filtered and evaporated to 11.5 g of an oil. This oil was purified by HPLC (silica, 20% ethyl acetate in dichloromethane) to give 3.8 g of desired product as a solid. This material was converted to the hydrochloride salt and twice recrystallized from isopropanol-ether to give 3.3 g of crystals, d 139°-140° C.

Workup

  1. temperaturethe reaction mixture was cooled
  2. extractionextracted with ethyl acetate
  3. extractionThe organic extract
  4. washwas washed with water and saturated sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customevaporated to 11.5 g of an oil
  8. customThis oil was purified by HPLC (silica, 20% ethyl acetate in dichloromethane)

Sources & evidence

ORD record
ord-f3c143c81dfd4a2c9c83112eb71d9603
Source dataset
uspto-grants-1993_03
Patent number
US05194618

Reaction notes

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