Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Adamantanecarbonyl chloride | HCID 98915 | — |
| Reactant | HCID 131717708 | HCID 131717708 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131717711 | HCID 131717711 | 71% |
Reaction Steps
A solution of 1-adamantanecarbonyl chloride (0.159 g, 0.000804 mol) in methylene chloride (2 ml) was added to a mixture of N2-[4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-ylthio]-1-oxobutyl]-L-lysine, methyl ester hydrobromide (0.5 g, 0.000804 mol), triethyl amine (0.24 g, 0.0024 mol) and methylene chloride (20 ml) at ambient temperature under a nitrogen atmosphere. The reaction mixture was stirred for 2 hours, poured into water and extracted with ethyl acetate. The combined organic layer was washed with saturated aqueous ammonium chloride, water, brine, dried over magnesium sulfate and concentrated to give a foam. The foam was purified by flash chromatography on silica gel (50 ml) eluting ethyl acetate to give the title compound (0.4 g, 0.00057 mol, 71% yield) as a white foam, mp 98°-104°. 1H NMR (DMSO-d6) δ8.22(d, 1H), 7.35-7.25(m, 5H), 6.87(d, 4H), 4.2-4.12(m, 1H), 3.75(s, 6H), 3.57(s, 3H), 3.1-2.93(m, 4H), 2.27(t, 2H), 1.97-1.5(m, 19H), 1.37-1.17(m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05179117 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-32bc47cc35f8487098eafafe29de2d57 |
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| Source note | uspto-grants-1993_01 |
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