Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfone | HCID 6213 | — |
| Reactant | Chloroformamidinium chloride | HCID 3084509 | — |
| Reactant | methyl 2-Acetamido-3-[2-[(2R)-2-[[3-(4-aminophenyl)benzoyl]amino]-4-benzyloxycarbonylbutoxy]-4-cyanophenyl]acrylate Trifluoroacetate | HCID 69142761 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178499878 | HCID 178499878 | — |
Reaction Steps
A mixture of 340 mg (0.52 mmol) of methyl 2-acetamido-3-[2-[(2R)-2-[[3-(4-aminophenyl)benzoyl]amino]-4-benzyloxycarbonylbutoxy]-4-cyanophenyl]acrylate trifluoroacetate, 430 mg (3.74 mmol) of chloroformamidine hydrochloride and 2.0 g of dimethyl sulfone was stirred at 120° C. for 2 hours. Water was added to the reaction mixture. After washing with ethyl acetate, the aqueous layer was freeze-dried and purified by the reversed phase HPLC in the same manner as that in step 5 in Example 1 to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06710056B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-08fbdee52c4a49f6a3a13adebffe294a |
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| Source note | uspto-grants-2004_03 |
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