Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | HCID 178454193 | HCID 178454193 | — |
| Product | HCID 178454181 | HCID 178454181 | — |
Reaction Steps
N-Boc-D-Arginine hydrochloride (100 mg, 0.3 mmol) was coupled with benzylamine (40 uL, 0.4 mmol) using the mixed anhydride method described in Example 322 to give N-Boc-D-arginine benzylamide. The Boc group was removed by treatment with 4 M hydrochloric acid in dioxane for 1 h. The resulting D-arginine benzylamide was coupled to N-Boc-(N-methyl)phenylalanyl-lysyl(N-epsilon-Boc)-prolyl-{(2R)-2-amino-3-cyclohexylpropanoyl}-{(2S)-2-amino-3-cyclohexylpropanoyl}-OH, which was prepared as described in Example 322, using 1-(3-dimethyl-aminopropyl)-3-ethyl carbodiimide hydrochloride in dimethylformamide using the method described in Example 322. The crude product was deprotected with 50% trifluoroacetic acid in methylene chloride. The material thus obtained was purified by HPLC as described in Example 2 to give the title compound in 26% overall yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05386011 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-ae9fbdc2004b4741a1e5ffe8d12666e5 |
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| Source note | uspto-grants-1995_01 |
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