HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-((tert-Butoxycarbonyl)amino)pyrimidine-5-carboxylic acid → HCID 58933876, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-((tert-Butoxycarbonyl)amino)pyrimidine-5-carboxylic acid | HCID 21471626 | — |
| Reactant | [1-(2-Phenylethylsulfonyl)piperidin-4-yl]methanamine | HCID 22135729 | — |
| Product | HCID 58933876 | HCID 58933876 | — |
Reaction Steps
(5-{[1-(2-Phenyl-ethanesulfonyl)-piperidin-4-ylmethyl]-carbamoyl}-pyrimidin-2-yl)-carbamic acid tert-butyl ester was prepared from C-[1-(2-phenyl-ethanesulfonyl)-piperidin-4-yl]-methylamine and 2-tert-butoxycarbonylamino-pyrimidine-5-carboxylic acid (prepared by BOC protection of ethyl 2-amino-5-pyrimidine carboxylate [prepared as described by P. Schenone, et al., J. Heterocyclic Chem., 27:295–305(1990)] using di-tert-butyl dicarbonate and 4-dimethylaminopyridine in acetonitrile, followed by saponification with sodium hydroxide and neutralization with dilute aqueous HCl) as described in EXAMPLE 1, Step 2:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259157B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-573705340d2f4e6889962c636a247862 |
| Source note | uspto-grants-2007_08 |