HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boc-L-Valine → Ethyl 6-(((S)-3-((((S)-2-amino-3-methylbutanoyl)oxy)methyl)morpholino)methyl)-4-(2,4-dichlorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Reactant | Ethyl 4-(2,4-dichlorophenyl)-6-(((S)-3-(hydroxymethyl)morpholino)methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 73295635 | — |
| Product | Ethyl 6-(((S)-3-((((S)-2-amino-3-methylbutanoyl)oxy)methyl)morpholino)methyl)-4-(2,4-dichlorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 73296136 | 36% |
Reaction Steps
Ethyl 4-(2,4-dichlorophenyl)-6-(((S)-3-(hydroxymethyl)morpholino)methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1 g, 1.96 mmol) was reacted with (S)-2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid (0.83 g, 3.8 mmol) according to the procedure as described in Example 49 to give the title compound as a yellow solid (0.43 g, 36%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340538B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-6b9d82b565cf4ef5accb013e31a47ea3 |
| Source note | uspto-grants-2016_05 |