HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxypyrimidine → N-(5-(2-Phenylethyl)pyrimidin-4-yl)-L-phenylalanine Isopropyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxypyrimidine | HCID 20695 | — |
| Reactant | 4-Chloro-5-iodopyrimidine | HCID 11230204 | — |
| Reactant | propan-2-yl (2S)-2-amino-3-phenylpropanoate hydrochloride | HCID 15599949 | — |
| Product | N-(5-(2-Phenylethyl)pyrimidin-4-yl)-L-phenylalanine Isopropyl Ester | HCID 10318179 | — |
| Product | propan-2-yl (2S)-2-amino-3-phenylpropanoate hydrochloride | HCID 15599949 | — |
Reaction Steps
L-Phenylalanine isopropyl ester hydrochloride was prepared by Method LLL. 4(3H)-Pyrimidinone (Aldrich) was sequentially converted via Methods N and O to 4-chloro-5-iodopyrimidine. L-Phenylalanine isopropyl ester hydrochloride and 4-chloro-5-iodopyrimidine were coupled via Method P and the coupled product sequentially converted via Methods OOO and X to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005433B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-85cef34de15946eea65b444b4a602201 |
| Source note | uspto-grants-2006_02 |