HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276375Generated: October 29, 2026
4-Methylmorpholine → HCID 66705936, compound
https://huagongshe.com/reaction/2276375
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 5-Chloro-2-picolinic acid | HCID 2762872 | — |
| Reactant | 1,1-Dimethylethyl 3-(4-aminophenyl)-1-pyrrolidinecarboxylate | HCID 57365069 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66705936 | HCID 66705936 | 101.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09132136B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-b7215dbfc650433fa5786e72182c9ff8 |
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| Source note | uspto-grants-2015_09 |
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