HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid → Ethyl 6-(((R)-3-((((S)-2-aminobutanoyl)oxy)methyl)morpholino)methyl)-4-(2-bromo-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid | HCID 2755934 | — |
| Reactant | Ethyl 4-(2-bromo-4-fluorophenyl)-6-(((S)-3-(hydroxymethyl)morpholino)methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 118107606 | — |
| Product | Ethyl 6-(((R)-3-((((S)-2-aminobutanoyl)oxy)methyl)morpholino)methyl)-4-(2-bromo-4-fluorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 118107506 | 31.2% |
Reaction Steps
Ethyl 4-(2-bromo-4-fluorophenyl)-6-(((S)-3-(hydroxymethyl)morpholino)methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1 g, 1.9 mmol) was reacted with (S)-2-((tert-butoxycarbonyl)amino)butanoic acid (0.61 g, 3 mmol) according to the procedure as described in Example 49 to give the title compound as yellow oil (0.37 g, 31%). 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-0cf949683c644b04b6c2f5ba6b4ed1bb |
| Source note | uspto-grants-2016_05 |