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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55886Generated: October 30, 2026

Morpholine → [2-(Morpholine-4-carbonyl)-pyridin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/55886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(((Tert-butoxy)carbonyl)amino)pyridine-2-carboxylic acidHCID 49760372—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product[2-(Morpholine-4-carbonyl)-pyridin-4-yl]-carbamic acid tert-butyl esterHCID 9035678393.5%

Reaction Steps

To a solution of 4-tert-butoxycarbonylamino-pyridine-2-carboxylic acid (43) (800 mg, 3.2 mmol) in CHCl3 was added morpholine (0.4 mL, 3.8 mmol), HOBT (857 mg, 6.3 mmol), EDC.HCl (1.2 g, 6.3 mmol) and DIPEA (0.8 mL, 4.8 mmol), and stirred at rt for 16 h. The reaction mixture was diluted with water and extracted with 10% MeOH/CHCl3. The organic layer was washed with water, dried over Na2SO4 and evaporated to give compound 44 (920 mg, 92%) as a white solid; (m/z): 308 [MH]+; 1H NMR (400 MHz, CDCl3): δ 8.40 (1H, d, J=5.6 Hz), 7.57 (1H, d, J=2.0 Hz), 7.54 (1H, d, J=5.6 Hz), 6.98 (1H, br s), 3.79 (4H, m), 3.67-3.66 (4H, m), 1.53 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09433622B2
Source datasetuspto-grants-2016_09
ORD IDord-64536afbf0dd4ae790a618f465ca584b
Source noteuspto-grants-2016_09