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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276375Generated: October 29, 2026

4-Methylmorpholine → HCID 66705936, compound

https://huagongshe.com/reaction/2276375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant5-Chloro-2-picolinic acidHCID 2762872—
Reactant1,1-Dimethylethyl 3-(4-aminophenyl)-1-pyrrolidinecarboxylateHCID 57365069—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66705936HCID 66705936101.2%

Reaction Steps

To a stirred suspension of (RS)-tert-butyl 3-(4-aminophenyl)pyrrolidine-1-carboxylate (200 mg, CAS 908334-28-1) in DMF (10 ml) were added sequentially N-methylmorpholine (0.22 ml), TBTU (490 mg) and 5-chloro-2-pyridine carboxylic acid (180 mg) and the mixture was stirred at room temperature for 90 min. The mixture was then diluted with ethyl acetate and washed sequentially with 1 M aq. hydrochloric acid and with saturated brine. The phases were separated and the organic phase was dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (SiO2; gradient: heptane/EtOAc) to give (RS)-3-{4-[(5-chloro-pyridine-2-carbonyl)-amino]-phenyl}-pyrrolidine-1-carboxylic acid tert-butyl ester (310 mg, quant.) as a white solid. MS (ISP): 421.3 ([M+NH4]+), 419.2 ([M+NH4]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132136B2
Source datasetuspto-grants-2015_09
ORD IDord-b7215dbfc650433fa5786e72182c9ff8
Source noteuspto-grants-2015_09