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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854312Generated: October 31, 2026

2-((tert-Butoxycarbonyl)amino)pyrimidine-5-carboxylic acid → HCID 58933876, compound

https://huagongshe.com/reaction/854312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((tert-Butoxycarbonyl)amino)pyrimidine-5-carboxylic acidHCID 21471626—
Reactant[1-(2-Phenylethylsulfonyl)piperidin-4-yl]methanamineHCID 22135729—
ProductHCID 58933876HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259157B2
Source datasetuspto-grants-2007_08
ORD IDord-573705340d2f4e6889962c636a247862
Source noteuspto-grants-2007_08