N,N-Dimethylethylenediamine → HCID 67388435, compound

HRID 905691Notes

Reaction equation

HRID 905691 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][NH:10][C:11]2[N:16]=[C:15]([NH:17][C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=3)[C:14]([C:25]([OH:27])=O)=[CH:13][N:12]=2)=[CH:4][CH:3]=1.CCN=C=NCCCN(C)C.Cl.C1C=CC2N(O)N=NC=2C=1.[CH3:50][N:51]([CH3:55])[CH2:52][CH2:53][NH2:54]>O.CN(C=O)C>[CH3:50][N:51]([CH3:55])[CH2:52][CH2:53][NH:54][C:25]([C:14]1[C:15]([NH:17][C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=2)=[N:16][C:11]([NH:10][CH2:9][CH2:8][C:5]2[CH:6]=[CH:7][C:2]([OH:1])=[CH:3][CH:4]=2)=[N:12][CH:13]=1)=[O:27]

Participants

7

Procedure

A 4 ml portion of DMF solution containing 352 mg of 2-{[2-(4-hydroxyphenyl)ethyl]amino}-4-[(3-methylphenyl)amino]pyrimidine-5-carboxylic acid was mixed with 223 mg of WSC hydrochloride, 157 mg of HOBt and 103 mg of 2-dimethylaminoethylamine, followed by stirring overnight at room temperature. The reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layer was washed with saturated brine and then the solvent was evaporated. The resulting residue was purified by a silica gel column chromatography (chloroform:methanol:aqueous ammonia) and then recrystallized (hexane-ethyl acetate) to obtain 291 mg of N-(2-dimethylaminoethyl)-2-{[2-(4-hydroxyphenyl)ethyl]amino}-4-[(3-methylphenyl)amino]pyrimidine-5-carboxamide as colorless crystals.

Workup

  1. extractionextracted with ethyl acetate
  2. washThe organic layer was washed with saturated brine
  3. customthe solvent was evaporated
  4. customThe resulting residue was purified by a silica gel column chromatography (chloroform:methanol:aqueous ammonia)
  5. customrecrystallized (hexane-ethyl acetate)

Sources & evidence

ORD record
ord-25bc2c382cf0445089ab5cf11bbdcc78
Source dataset
uspto-grants-2011_09
Patent number
US08012959B2

Reaction notes

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