Methanesulfonic Acid → Entinostat

HRID 430027Notes

Reaction equation

HRID 430027 reaction equation
CN1CCN(C)C1=O.[N:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][O:16][C:17]([NH:19][CH2:20][C:21]2[CH:29]=[CH:28][C:24]([C:25]([OH:27])=O)=[CH:23][CH:22]=2)=[O:18])[CH:10]=1.[C:30]1([NH2:37])[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=1[NH2:36].CS(O)(=O)=O>O>[NH2:36][C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=1[NH:37][C:25](=[O:27])[C:24]1[CH:23]=[CH:22][C:21]([CH2:20][NH:19][C:17]([O:16][CH2:15][C:11]2[CH:10]=[N:9][CH:14]=[CH:13][CH:12]=2)=[O:18])=[CH:29][CH:28]=1

Participants

6

Reactant 4

HCID 6395Methanesulfonic AcidHCID 66611,3-Dimethyl-2-imidazolidinoneHCID 7243O-PhenylenediamineHCID 98173384-((((Pyridin-3-ylmethoxy)carbonyl)amino)methyl)benzoic acid

Product 1

HCID 4261EntinostatYield 72%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

7.78 g (48 mmole) of N,N′-carbonyldiimidazole were added to a 1,3-dimethyl-2-imidazolidinone (50 g) suspension including 11.45 g (40 mmole) of 4-[N-(pyridin-3-ylmethoxycarbonyl)aminomethyl]benzoic acid. After stirring at room temperature for 2 hours, 17.30 g (0.16 mole) of 1,2-phenylenediamine were added to the solution. After cooling to 2° C., 9.60 g (0.1 mole) of methanesulfonic acid were added dropwise. After stirring for 2 hours, water was added, and the deposited solid was collected by filtration. Purification was then carried out through silica gel column chromatography to obtain 10.83 g (yield: 72%) of N-(2-aminophenyl)-4-[N-(pyridin-3-ylmethoxycarbonyl)aminomethyl]benzamide.

Workup

  1. temperatureAfter cooling to 2° C.
  2. stirringAfter stirring for 2 hours
  3. filtrationthe deposited solid was collected by filtration
  4. customPurification

Sources & evidence

ORD record
ord-bf1799b7972640e7afdde4443f625ed4
Source dataset
uspto-grants-2001_11
Patent number
US06320078B1

Reaction notes

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