Water → HCID 59809683, compound

HRID 2114342Notes

Reaction equation

HRID 2114342 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([NH:15][CH3:16])[CH2:9][N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:5]=[CH:6][CH:7]=1.[Cl:17][C:18]1[CH:19]=[C:20]([N:25]([CH3:30])[CH2:26][C:27]([OH:29])=O)[CH:21]=[CH:22][C:23]=1[Cl:24].C(N(CC)CC)C.O>CN(C)C=O>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([N:15]([CH3:16])[C:27](=[O:29])[CH2:26][N:25]([C:20]2[CH:21]=[CH:22][C:23]([Cl:24])=[C:18]([Cl:17])[CH:19]=2)[CH3:30])[CH2:9][N:10]2[CH2:11][CH2:12][CH2:13][CH2:14]2)[CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

[1-(3-Bromophenyl)-2-(1-pyrrolidinyl)ethyl]methylamine (0.65 g, 2.30 mmol) was added to a solution of N-(3,4-dichlorophenyl)-N-methylglycine (0.65 g, 2.30 mmol), (benzotriazol-1-yloxy) tris(dimethylamino) phosphonium-hexaflurophosphate (BOP) (1.52 g, 3.40 mmol) and triethylamine (TEA) (0.70 g, 6.90 mmol) in N,N-dimethyl-formamide (DMF) (10 mL). The reaction mixture was stirred at RT for 12 h. Water (10 mL) was then added an the crude compound precipitated, was filtered and crystallized from ether and hexane to give the title compound as an off-white solid (0.62 g, 54%). MS (ES) m/e 499[M+H]+.

Workup

  1. customprecipitated
  2. filtrationwas filtered
  3. customcrystallized from ether and hexane

Sources & evidence

ORD record
ord-047573580d784aea88b794aef9806f67
Source dataset
uspto-grants-2008_10
Patent number
US07432258B2

Reaction notes

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