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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896651Generated: November 3, 2026

4-Amino-1-Boc-piperidine → HCID 178452095, compound

https://huagongshe.com/reaction/1896651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantPyrimidine-4-carboxaldehydeHCID 11412355—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 178452095HCID 178452095—

Reaction Steps

Pyrimidine-4-carbaldehyde (C12) (23.00 g, 212.8 mmol) was added to a mixture of tert-butyl 4-aminopiperidine-1-carboxylate (42.61 g, 212.8 mmol) in tert-butyl methyl ether (1.52 L). After 2.5 hours, the reaction was filtered, and the filtrate was concentrated in vacuo to provide an amber oil, which was generally taken directly to the following step. Yield: 56.30 g, 193.9 mmol, 91%. 1H NMR (400 MHz, CDCl3) partial spectrum, characteristic peaks: δ 1.49 (s, 9H), 7.95 (dd, J=5.2, 1.5 Hz, 1H), 8.36 (s, 1H), 8.81 (d, J=5.2 Hz, 1H), 9.28 (d, J=1.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518944B2
Source datasetuspto-grants-2013_08
ORD IDord-ea119fc574d64493825f55c21f4db86f
Source noteuspto-grants-2013_08