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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096630Generated: November 3, 2026

4-Methylmorpholine → HCID 66791505, compound

https://huagongshe.com/reaction/1096630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-(1,1-Dimethylethyl) (3R)-1,3-piperidinedicarboxylateHCID 643516—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 66791978HCID 66791978—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66791505HCID 66791505155.8%

Reaction Steps

5-Methoxy-N1-(3-methoxypropyl)benzene-1,2-diamine (42B) (1.81 mmol, 380 mg) in DMF (20 mL) was added (R)-(−)-N-Boc-nipecotic acid (2.35 mmol, 541 mg) and N-methylmorpholine (5.43 mmol, 0.60 mL). The reaction mixture was stirred at rt for 5 min and then added HATU (2.72 mmol, 1.03 g) and kept stirring at rt overnight. The reaction mixture was poured into H2O, extracted with EtOAc. The extract was washed with H2O, NaHCO3, brine, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo and purified by flash chromatography (silica gel, EtOAc-hexane: 1:2) to afford (R)-tert-butyl 3-(4-methoxy-2-(3-methoxypropylamino)phenylcarbarnoyl)piperidine-1-carboxylate (42C) (2.82 mmol, 1.19 g, three-step yield: 80.6%). ESI-MS: m/z 422.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138168B1
Source datasetuspto-grants-2012_03
ORD IDord-22d9f964df2349c9b955f4ce325be205
Source noteuspto-grants-2012_03