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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096637Generated: November 3, 2026

4-Methylmorpholine → HCID 66786129, compound

https://huagongshe.com/reaction/1096637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant(R)-3-((tert-butoxycarbonyl)amino)-4-(naphthalen-2-yl)butanoic acidHCID 7021578—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 66791505HCID 66791505—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66786129HCID 6678612916.7%

Reaction Steps

Methyl 1-(3-methoxypropyl)-2-(piperidin-3-yl)-1H-benzo[d]imidazole-7-carboxylate (42C) (0.36 mmol, 120 mg) in DMF (10 mL) was added (R)-3-(tert-butoxycarbonylamino)-4-(naphthalen-2-yl)butanoic acid (0.40 mmol, 132 mg) and N-methylmorpholine (1.44 mmol, 0.16 mL). The reaction mixture was stirred at rt for 5 min and then added HATU (0.40 mmol, 152 mg) 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 preparative LC/MS (40-70% CH3CN in H2O) to afford methyl 2-(1-((R)-3-(tert-butoxycarbonylamino)-4-(naphthalen-2-yl)butanoyl)piperidin-3-yl)-1-(3-methoxypropyl)-1H-benzo[d]imidazole-7-carboxylate (44D) (0.06 mmol, 40 mg, yield: 16.7%). ESI-MS: m/z 643.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138168B1
Source datasetuspto-grants-2012_03
ORD IDord-731d3347a1af405181ddd5535c669419
Source noteuspto-grants-2012_03