HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720206Generated: October 28, 2026
1,2-Dichloroethane → Pyrrolidine-2-carboxylic acid {1-(4-fluorobenzyl)-2-[2-methoxy-methyl-4-(1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-piperazin-1-yl]-2-oxo-ethyl}-amide
https://huagongshe.com/reaction/720206
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Trifluoroacetate | HCID 84468 | — |
| Reactant | 2-{1-(4-Fluorobenzyl)-2-[2-methoxymethyl-4-(1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-piperazin-1-yl]-2-oxo-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 69587859 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Pyrrolidine-2-carboxylic acid {1-(4-fluorobenzyl)-2-[2-methoxy-methyl-4-(1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-piperazin-1-yl]-2-oxo-ethyl}-amide | HCID 131726051 | 54% |
Reaction Steps
Crude 2-{1-(4-fluorobenzyl)-2-[2-methoxymethyl-4-(1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-piperazin-1-yl]-2-oxo-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester, 67, is dissolved in 4M hydrogen chloride in dioxane (10 mL) and stirred at room temperature for 1 hour. 1,2-dichloroethane (10 mL) is added. Removal of solvents in vacuo gives the crude hydrogen chloride salt of product which is then purified by preparative HPLC to afford 0.22 g (54% yield) of the desired product as the trifluoroacetate salt. A small amount of product is converted into free base by treating with NaHCO3 to obtain NMR spectra. 1H NMR (CDCl3, δ): 7.80–7.60 (m, 4H), 7.45–7.25 (m, 3H), 7.18–7.00 (m, 2H), 7.00–6.85 (m, 2H), 6.32–6.28 (m, 0.5H), 5.08–4.92 (m, 1H), 4.78–4.69 (,0.5H), 4.10 (d, J=13.0 Hz, 0.5H), 3.70–3.58 (m, 1H), 3.58–3.15 (m, 8H), 2.98–2.46 (m, 11H), 2.28–2.15 (m, 0.5H), 2.15–1.50 (m, 8H). HRFAB(positive) m/e 604.2399 calculated for C34H42FN5O4 (M+H)+, Found 604.3292.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132539B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-2d6ba40ff5a246af9996c8a634c368cf |
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| Source note | uspto-grants-2006_11 |
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