Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Reactant | HCID 67642996 | HCID 67642996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70199112 | HCID 70199112 | 19.9% |
Reaction Steps
To a solution of the product from Step G (63 mg, 0.17 mmol) in 2.5 mL of THF at 0° C. was added triethylamine (0.15 mL, 1.0 mmol), followed by triphosgene (31 mg, 0.10 mmol). The reaction was stirred at 0° C. for 1.5 hour, then poured into EtOAc and washed with sat. aq. NaHCO3 and brine. The solution was dried (Na2SO4), filtered, and concentrated in vacuo. The product was taken up in methanol and injected onto a preparative HPLC column and purified with a mixed gradient of 25%-55% acetonitrile/0.1% TFA; 75%-45% 0.1% aqueous TFA over 50 minutes. After concentration in vacuo, the resultant product was partitioned between dichloromethane and aq. NaHCO3 soln., and the aqueous phase was extracted with CH2Cl2. The organic solution was washed with brine, dried (Na2SO4), filtered, and concentrated to dryness to provide the product free base, which was taken up in CH2Cl2 and treated with excess 1M HCl/ether solution. After concentrated in vacuo, the titled product (9.3 mg) was isolated as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780492 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-bcba43788ce7499faae1927deeb2ded2 |
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| Source note | uspto-grants-1998_07 |
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