Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine tert-butyl ester hydrochloride | HCID 2725036 | — |
| Reactant | HCID 19390818 | HCID 19390818 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19390813 | HCID 19390813 | — |
Reaction Steps
2-(5-Benzyloxycarbonylamino-6-oxo-2-phenyl-1,6-dihydropyrimidin-1-yl)-N-[3,3-difluoro-1-isopropyl-2-hydroxy-3-[N-(tert-butoxycarbonylmethyl)carbamoyl]propyl]acetamide. To a solution of the product described at Example 1.b. (1.05 g) in tetrahydrofuran (17 mL) was added triethylamine (0.82 mL) and glycine tert-butylester hydrochloride (0.990 g). After 18 hours, additional triethylamine (0.30 mL) and glycine tert-butylester hydrochloride (0.33 g) were added. The additions were repeated after 1 day, and the reaction mixture stirred for 1 day. The mixture was evaporated and the solids were triturated with water, collected by filtration, washed (water, ether, hexane), and dried under vacuum to yield the title compound as a white powder; TLC: Rf =0.47, chloroform:methanol (97:3); m/z=672(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05441960 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-060b3a7c01854bd4b2aa86328b39d768 |
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| Source note | uspto-grants-1995_08 |
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