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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502391Generated: November 3, 2026

Pyrimidine-5-carboxylic acid → HCID 68456978, compound

https://huagongshe.com/reaction/502391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrimidine-5-carboxylic acidHCID 78346—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 68455584HCID 68455584—
ProductHCID 68456978HCID 68456978—

Reaction Steps

In analogy to the procedure described in example 50k), pyrimidine-5-carboxylic acid piperidin-4-ylamide [prepared in analogy to the procedures described in examples 50 h) and 50i) by condensation of pyrimidine-5-carboxylic acid with 4-amino-piperidine-carboxylic acid tert-butyl ester to give 4-[(pyrimidine-5-carbonyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester followed by Boc cleavage with trifluoroacetic acid] was reacted with 3,5-diethoxy-4-fluoro-benzaldehyde (example 50 g), sodium cyano-borohydride, N-ethyl-diisopropylamine and acetic acid in ethanol at 50° C. to yield the title compound as light yellow solid. MS: 403.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772253B2
Source datasetuspto-grants-2010_08
ORD IDord-1c3abb2f245c4450a0844618133bb875
Source noteuspto-grants-2010_08