1-Hydroxybenzotriazole → HCID 86615147, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 4
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
- customthe organic layer was separated
- washThe resulting organic layer was washed with brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered through a silica gel pad (Chromatorex NH)
- concentrationThe filtrate was concentrated under reduced pressure
- 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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