Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 11447897 | HCID 11447897 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11207924 | HCID 11207924 | 95% |
Reaction Steps
Phosgene (28.9 kg, 291.9 mol) was added to (2R)-2-cyclohexyl-2-[(2-ethoxy-2-oxoethyl) amino]ethanoic acid (44.2 kg, 182 mol, obtained analogously to the method described in step (c) (Alternative A) above) in tetrahydrofuran (340 kg) at 40° C. over one hour. The reaction was deemed to be complete after a further hour. The mixture was concentrated at reduced pressure. The residue was diluted with tetrahydrofuran (272.6 kg) and the pH was adjusted at 0° C. to 6.5 with N-methylmorpholine (15.3 kg). The reaction was continued for a further 45 minutes. HCI/dioxane (0.34 kg) was then added and the residue was filtered through Celite®. The filter cake was washed twice with tetrahydrofuran. The combined filtrates were concentrated at reduced pressure at 20° C. To the residue was added heptane (250 kg), and the mixture was concentrated again. To the resultant residue further heptane (81 kg) was added. The temperature was adjusted to 0° C. and the mixture was allowed to crystallise for five hours. The crystals were filtered, washed (3×30 kg heptane) and dried (low pressure, 20° C.), to yield 46 kg (95%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518434B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-4362ee7108a94b1db7699931f20c8cf0 |
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| Source note | uspto-grants-2003_02 |
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