Hydrochloric Acid → HCID 11375602, compound

HRID 1618301Notes

Reaction equation

HRID 1618301 reaction equation
C[O-].[Na+].C(O[C:9]([C:11]1[N:12]=[CH:13][C:14]2[C:19]([C:20]=1[OH:21])=[CH:18][CH:17]=[C:16]([O:22][C:23]1[CH:28]=[CH:27][C:26]([NH:29][S:30]([C:33]3[CH:38]=[CH:37][C:36]([CH3:39])=[CH:35][CH:34]=3)(=[O:32])=[O:31])=[CH:25][CH:24]=1)[CH:15]=2)=[O:10])CCC.[NH2:40][CH2:41][C:42]([OH:44])=[O:43].Cl>CO>[OH:21][C:20]1[C:19]2[C:14](=[CH:15][C:16]([O:22][C:23]3[CH:24]=[CH:25][C:26]([NH:29][S:30]([C:33]4[CH:38]=[CH:37][C:36]([CH3:39])=[CH:35][CH:34]=4)(=[O:32])=[O:31])=[CH:27][CH:28]=3)=[CH:17][CH:18]=2)[CH:13]=[N:12][C:11]=1[C:9]([NH:40][CH2:41][C:42]([OH:44])=[O:43])=[O:10]

Participants

6

Procedure

To a solution of 1.85 ml of 0.5 M sodium methoxide in methanol was added 42 mg of 4-Hydroxy-7-[4-(toluene-4-sulfonylamino)-phenoxy]-isoquinoline-3-carboxylic acid butyl ester and 70 mg of glycine. The resultant mixture was heated at reflux temperature for 24 hours and then cooled to room temperature. The reaction was poured into a 0.2 N HCl aqueous solution and then extracted three times with ethyl acetate. The organic fractions were dried over anhydrous sodium sulfate and concentrated to 41 mg of a white solid; MS (+): m/z 508.10 (M+1).

Workup

  1. temperatureat reflux temperature for 24 hours
  2. extractionextracted three times with ethyl acetate
  3. dry with materialThe organic fractions were dried over anhydrous sodium sulfate
  4. concentrationconcentrated to 41 mg of a white solid

Sources & evidence

ORD record
ord-3779da2a99854d19b06c42dd142a3d0e
Source dataset
uspto-grants-2014_07
Patent number
US08765956B2

Reaction notes

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