Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 66842809 | HCID 66842809 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66843305 | HCID 66843305 | — |
Reaction Steps
Methyl N-{[4-((2R,3R)-1-(4-fluorophenyl)-3-{[2-(4-fluorophenyl)-2-oxoethyl]thio}-4-oxoazetidin-2-yl)phenoxy]acetyl}glycyl-L-phenylalaninate (20 mg, 0.029 mmol) was dissolved in 1.6 ml MeOH and 0.2 ml H2O. Et3N (0.2 ml, 1.44 mmol) was added and the mixture was stirred overnight. The mixture was heated to 80° C. for 7 h. The mixture was purified by preparative HPLC using a C8 column (25×300 mm). A gradient from 20% to 40% MeCN in 0.1 M ammonium acetate was used as mobile phase. The product fraction was concentrated and lyophilized to yield 7 mg (36%). M/z: 688.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07871998B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-fbfe5a7528da4cd9a92fc71a95f3a0b6 |
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| Source note | uspto-grants-2011_01 |
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