Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ninhydrin | HCID 10236 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 72524391 | HCID 72524391 | — |
| Reactant | acetic anhydride DMF | HCID 86761394 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | dichloromethane N-methyl-2-pyrrolidone | HCID 19383075 | — |
| Product | Tacrolimus | HCID 445643 | — |
Reaction Steps
The syrup obtained in Example 1 was centrifuged with benzene and concentrated under reduced pressure, and dissolved in a mixed solvent of methylene chloride/N-methyl-2-pyrrolidone (4/1) (0.3 ml), and WSC (1.44 mg, 7.5 μmol) and 1-hydroxybenzotriazole (1.01 mg, 7.5 μmol) were added. This solution was added to 10 μl of TOYO-Pearl resin (TSKgel AF-amino; 0.01 mmol amine is present in 100 μl) and shaken at room temperature overnight. After completion of the reaction, the resin was thoroughly washed with a mixed solvent of methylene chloride/N-methyl-2-pyrrolidone (4/1), and DMF, and the percent condensation yield was determined by the ninhydrin test (about 29%). A mixed solution of acetic anhydride/DMF (1/4) (0.3 ml) was added to the resin obtained, and this was followed by shaking at room temperature for 30 minutes. After completion of the reaction, the resin was thoroughly washed with methylene chloride, dimethylformamide (DMF) and 20% aqueous ethanol, and this resin was used as the affinity resin in the subsequent experiments.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645614B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-667291f776064bb6b6d0d90a4de81add |
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| Source note | uspto-grants-2010_01 |
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