1-Hydroxybenzotriazole → HCID 86615147, compound

HRID 1009427Notes

Reaction equation

HRID 1009427 reaction equation
C1C=C[C:4]2[N:9](O)N=[N:7][C:5]=2C=1.C(N(C(C)C)CC)(C)C.[CH3:20][O:21][C:22]1[CH:23]=[C:24](/[CH:34]=[CH:35]/[C:36]([OH:38])=O)[CH:25]=[CH:26][C:27]=1[N:28]1[CH:32]=[C:31]([CH3:33])[N:30]=[CH:29]1.Cl.NCC#N>CN(C=O)C.O.C(OCC)(=O)C.C(Cl)CCl>[C:5]([CH2:4][NH:9][C:36](=[O:38])/[CH:35]=[CH:34]/[C:24]1[CH:25]=[CH:26][C:27]([N:28]2[CH:32]=[C:31]([CH3:33])[N:30]=[CH:29]2)=[C:22]([O:21][CH3:20])[CH:23]=1)#[N:7]

Participants

9

Procedure

EDC (4.48 g), HOBT (3.14 g) and IPEA (6.76 mL) were sequentially added to a solution of (E)-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]acrylic acid (2 g) and aminoacetonitrile hydrochloride (1.08 g) in DMF (25 mL), and the reaction solution was stirred at room temperature for five hours. Ethyl acetate and water were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine and then dried over anhydrous sodium sulfate and filtered through a silica gel pad (Chromatorex NH). The filtrate was concentrated under reduced pressure. The residue was crystallized (heptane-ethyl acetate-methanol system) to obtain 1.24 g of the title compound. The property values of the compound are as follows.

Workup

  1. customthe organic layer was separated
  2. washThe resulting organic layer was washed with brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered through a silica gel pad (Chromatorex NH)
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. customThe residue was crystallized (heptane-ethyl acetate-methanol system)

Sources & evidence

ORD record
ord-32bb05482edc41a08c4e66b8f263704b
Source dataset
uspto-grants-2011_07
Patent number
US07973033B2

Reaction notes

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