Hydrochloric Acid → HCID 15100255, compound

HRID 1708166Notes

Reaction equation

HRID 1708166 reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[CH:14]=[CH:13][C:7]([O:8][CH2:9][C:10]([OH:12])=[O:11])=[CH:6][CH:5]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:21][N:22]1[CH:26]=[C:25]([S:27](Cl)(=[O:29])=[O:28])[N:24]=[CH:23]1.Cl>O>[CH3:21][N:22]1[CH:26]=[C:25]([S:27]([NH:1][CH2:2][CH2:3][C:4]2[CH:5]=[CH:6][C:7]([O:8][CH2:9][C:10]([OH:12])=[O:11])=[CH:13][CH:14]=2)(=[O:29])=[O:28])[N:24]=[CH:23]1

Participants

6

Conditions

Temperature
80 °C

Procedure

6.3 g (32 mmol) of 4-(2-aminoethyl)phenoxyacetic acid are added to a solution of 9.7 g (79 mmol) of potassium carbonate in 50 ml of water and the mixture is stirred for 5 minutes. A suspension of 5.8 g (32 mmol) of 1-methyl-4-imidazolesulfonyl chloride from Example C-1 in 20 ml of water is slowly added to this suspension. The mixture is heated to 80° C. and stirred at this temperature for 2 hours. After cooling to room temperature, the reaction solution is acidified to pH 4 using 2N hydrochloric acid. The precipitate deposited is separated off, washed several times with water and recrystallized from dilute acetic acid in order to give the title compound of melting point 203°-204° C.

Workup

  1. additionis slowly added to this suspension
  2. stirringstirred at this temperature for 2 hours
  3. temperatureAfter cooling to room temperature
  4. customThe precipitate deposited is separated off
  5. washwashed several times with water
  6. customrecrystallized from dilute acetic acid in order

Sources & evidence

ORD record
ord-524412fae763444b949f991a072d7403
Source dataset
uspto-grants-1994_10
Patent number
US05356922

Reaction notes

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