HCID 86618879, compound → HCID 86618878, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][C:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([CH2:15][CH:16]([CH:30]([CH3:32])[CH3:31])[CH2:17][CH:18]([NH:22][C:23](=[O:29])[O:24][C:25]([CH3:28])([CH3:27])[CH3:26])[CH:19]3[CH2:21][O:20]3)[CH:13]=2)[N:8]([CH3:33])[CH:7]=1>C(O)(C)C.C(N)(C)C>[OH:20][CH:19]([CH:18]([NH:22][C:23](=[O:29])[O:24][C:25]([CH3:28])([CH3:26])[CH3:27])[CH2:17][CH:16]([CH2:15][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][CH:11]=1)[N:8]([CH3:33])[CH:7]=[C:6]2[CH2:5][CH2:4][CH2:3][O:2][CH3:1])[CH:30]([CH3:31])[CH3:32])[CH2:21][NH:8][CH:9]([CH3:14])[CH3:10]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 0.032 g of tert-butyl {3-[3-(3-methoxypropyl)-1-methyl-1H-indol-5-ylmethyl]-4-methyl-1-oxiranylpentyl}carbamate in 1 ml of isopropanol and 0.044 ml of isopropylamine is stirred at 70° C. On completion of reaction (TLC monitoring), the reaction mixture is concentrated by evaporation, and the residue is admixed with water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed successively with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is identified on the basis of the Rf value from the residue by means of flash chromatography (SiO2 60F).
Workup
- customOn completion of reaction (TLC monitoring)
- concentrationthe reaction mixture is concentrated by evaporation
- extractionextracted with tert-butyl methyl ether (2×)
- washThe combined organic phases are washed successively with water and brine
- dry with materialdried over sodium sulphate
- concentrationconcentrated by evaporation
Sources & evidence
- ORD record
- ord-a99df733095e4049ba8884cc8cb915f9
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07868036B2
Reaction notes
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