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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226383Generated: October 25, 2026

Ethyl Acetate → ethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinate

https://huagongshe.com/reaction/226383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
ReactantEthyl 5,6-DichloronicotinateHCID 16762519—
SolventWaterHCID 962—
Solvent1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Productethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinateHCID 68960873—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl 5,6-dichloronicotinate (10.0 g) and N,N-diisopropylethylamine (17.4 mL) in 1,3-dimethyl-2-imidazolidinone (100 mL) was added tert-butyl (3R)-3-amino-1-piperidinecarboxylate (10.9) at ambient temperature and the mixture was stirred at 100° C. for 9 hr. The reaction mixture was poured into a mixture of AcOEt and water. The separated organic layer was added ice-water and the mixture was adjusted to pH 3.5 with 1N-NCl. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated in vacuo to give ethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinate (16.74 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-189540655c5b42c18e5e1e88f126e5c4
Source noteuspto-grants-2009_07