HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612271Generated: October 30, 2026
Lithium Hydroxide → Benzyl(cis)-3-{[5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-yl]amino}-4-hydroxypyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1612271
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzyl(cis)-3-{[5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-yl]amino}-4-[(4-nitrobenzoyl)oxy]pyrrolidine-1-carboxylate | HCID 58583363 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl(cis)-3-{[5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-yl]amino}-4-hydroxypyrrolidine-1-carboxylate | HCID 58583263 | 50% |
Reaction Steps
To a solution of benzyl (cis)-3-{[5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-yl]amino}-4-[(4-nitrobenzoyl)oxy]pyrrolidine-1-carboxylate (3.17 g) in tetrahydofuran (38 ml) and methanol (3 ml) was added LiOH (1M(aq), 38 ml). The reaction mixture stirred 45 min and was poured into saturated sodium bicarbonate (100 ml). The aqueous layer was extracted ethyl acetate (2×200 ml), dried MgSO4, filtered and concentrated. MPLC chromatography on a biotage 40M column with 20-60% ethyl acetate/heptane provided the title compound as an oil (1.225 g, 50%): 1H NMR (400 MHz, CDCl3) δ) 7.50, 7.46-7.25, 5.18, 4.99, 4.89, 4.70, 4.51, 4.04, 3.75-3.59, 3.42-3.35, 2.70, 2.47, 2.19, 1.14; HRMS (FAB) calcd for C26H28Cl2N4O3+H 515.1616, found 515.1641. Anal. Calcd for C26H28Cl2N4O3: C, 60.59; H, 5.48; N, 10.87. Found: C, 60.32; H, 5.79; N, 10.54.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992087B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-21eec652d99d4b93bbcae980357a1364 |
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| Source note | uspto-grants-2006_01 |
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