HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine-3-carboxylic acid hydrochloride → 4-((6-(2-Chlorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine-3-carboxylic acid hydrochloride | HCID 45790954 | — |
| Reactant | Ethyl 6-(bromomethyl)-4-(2-chlorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 90043618 | — |
| Product | 4-((6-(2-Chlorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acid | HCID 90042616 | 45% |
Reaction Steps
Ethyl 6-(bromomethyl)-4-(2-chlorophenyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (2 g, 4.5 mmol) was reacted with morpholine-3-carboxylic acid hydrochloride (0.75 g, 4.5 mmol) according to the procedure as described in Example 1, Step C to give the title compound as a yellow solid (0.99 g, 45%). 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-db09c149ab7c42c2ba22da256cbcdafa |
| Source note | uspto-grants-2016_05 |