Diisopropylethylamine → HCID 178456942, compound

HRID 1620716Notes

Reaction equation

HRID 1620716 reaction equation
Cl.Cl.[CH2:3]([NH:6][C:7]1=[N:8][C:9](=[O:19])[S:10]/[C:11]/1=[CH:12]\[CH:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1)[C:4]#[CH:5].C(N(C(C)C)C(C)C)C.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.[Cl:53][C:54]1[CH:55]=[CH:56][C:57]2[O:61][C:60]([C:62](O)=[O:63])=[CH:59][C:58]=2[CH:65]=1>CN(C=O)C.O>[Cl:53][C:54]1[CH:55]=[CH:56][C:57]2[O:61][C:60]([C:62]([N:16]3[CH2:17][CH2:18][CH:13](/[CH:12]=[C:11]4/[C:7]([NH:6][CH2:3][C:4]#[CH:5])=[N:8][C:9](=[O:19])[S:10]/4)[CH2:14][CH2:15]3)=[O:63])=[CH:59][C:58]=2[CH:65]=1

Participants

7

Procedure

To a solution of (5Z)-4-(prop-2-yn-1-ylamino)-5-(piperidin-4-ylmethylidene)-1,3-thiazol-2(5H)-one dihydrochloride (200 mg) in DMF (3 mL) were added N-ethyl-N-(1-methylethyl)propan-2-amine (0.56 mL), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (283 mg), and 5-chlorobenzofuran-2-carboxylic acid (151 mg). The reaction mixture was stirred at room temperature overnight, water was added, the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate/heptane to give the title compound (57 mg).

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with water and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was recrystallized from ethyl acetate/heptane

Sources & evidence

ORD record
ord-0a21847baa524bc9ad118097d55007de
Source dataset
uspto-grants-2014_07
Patent number
US08772277B2

Reaction notes

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