Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-(2-(O-tolylamino)benzo[d]oxazol-6-yl)acetic acid | HCID 23508315 | — |
| Reactant | HCID 86592797 | HCID 86592797 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58778667 | HCID 58778667 | 97% |
Reaction Steps
In DMF (10 ml), a mixture of 2-(2-methylphenylamino)-6-benzoxazolylacetic acid (318 mg, 1.13 mmol), 4-((2S,4S)-4-acetoxy-2-pyrrolidinylmethoxy)benzoate (330 mg, 1.13 mmol), EDC•HCl (325 mg, 1.70 mmol), HOBt (230 mg, 1.70 mmol) and triethylamine (1.18 ml, 8.50 mmol) was stirred at room temperature for 21 hours. The reaction mixture was poured in ice water (30 ml), followed by extraction with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (silica gel: 40 g), whereby from chloroform/acetone (20/1) eluate fractions, the title compound (610 mg, 97%) was obtained as a colorless amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-3d8c89ffc1e2408eb3627d9077617b6e |
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| Source note | uspto-grants-2007_01 |
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