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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072176Generated: October 27, 2026

1,2-Dichloroethane → 4-methyl-5-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehyde

https://huagongshe.com/reaction/1072176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Formyl-3-methyl-1H-pyrrole-2-carboxylic acidHCID 15694078—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-methyl-5-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 2239098689%

Reaction Steps

To a solution of 5-formyl-3-methyl-1H-pyrrole-2-carboxylic acid (306.3 mg, 2 mmol) in DMF (5 mL) was added HOBt (324.3 mg, 2.4 mmol), EDC (460.1 mg, 2.4 mmol) and then morpholine (0.21 mL, 2.4 mmol). The mixture was stirred at room temperature under nitrogen for overnight. The reaction was diluted with ethyl acetate and washed with sodium bicarbonate. The aqueous layer was extracted several times with ethyl acetate. The combined organic layer was washed with brine, dried, concentrated and column chromatographed (MeOH/DCM) to give 395 mg (89%) of 4-methyl-5-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehyde as a light yellow foam solid. 1H NMR (360 MHz, DMSO-d6) δ 12.18 (br s, 1H, NH), 9.46 (s, 1H, CHO), 6.79 (s, 1H), 3.43 (m, 4H, 2×CH2), 2.29 (m, 4H, 2×CH2), 2.17 (s, 3H, CH3), 2.01 (s, 3H, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908930B2
Source datasetuspto-grants-2005_06
ORD IDord-3bd7ddd23770419ab9deb8aae352a710
Source noteuspto-grants-2005_06