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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323709Generated: October 25, 2026

4-Methylmorpholine → (s)-n-(1-Hydroxymethyl-2-phenylethyl)-1-methyl-2-indolecarboxamide

https://huagongshe.com/reaction/323709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1H-Indole-2-carboxylic acid, 1-methyl-HCID 27695—
Reactantphenylalaninol, (S)-HCID 447213—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product(s)-n-(1-Hydroxymethyl-2-phenylethyl)-1-methyl-2-indolecarboxamideHCID 6986174268.1%

Reaction Steps

To a stirred solution of 1-methyl-2-indolecarboxylic acid (100 mg, 0.57 mmol) in methylene chloride (1 mL) was added N-methylmorpholine (0.063 mL, 0.57 mmol) followed by (S)-(−)-2-amino-3-phenyl-1-propanol (86 mg, 0.57 mmol), 1-hydroxybenzotriazole hydrate (81 mg, 0.60 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (120 mg, 0.63 mmol). The resulting mixture was stirred at room temperature for 20 h. The reaction was diluted with methylene chloride and washed sequentially with 10% citric acid, saturated NaHCO3, water, and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to give a crude oil. Trituration of the crude oil with methanol and diethyl ether afforded the title compound (68%, 119.7 mg) as an off-white solid. MS (ES) m/e 309.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214856B1
Source datasetuspto-grants-2001_04
ORD IDord-ba43aa1208ed46849711ebd9f4436e12
Source noteuspto-grants-2001_04