HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370846Generated: October 31, 2026
Lithium Hydroxide → 5-(Benzyloxy)-6-((tert-butoxycarbonyl)amino)nicotinic Acid
https://huagongshe.com/reaction/2370846
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl 5-(benzyloxy)-6-((tert-butoxycarbonyl)amino)nicotinate | HCID 71144248 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 5-(Benzyloxy)-6-((tert-butoxycarbonyl)amino)nicotinic Acid | HCID 71144320 | — |
Reaction Steps
To a cooled (0° C.) stirred mixture of ethyl 5-(benzyloxy)-6-((tert-butoxycarbonyl)amino)nicotinate (1.2 g, 0.0032 mol) in EtOH:water (1:1, 12 mL), was added LiOH (154 mg, 0.0064 mol, Aldrich). The reaction mixture was stirred for 2 h at room temperature. After completion of the reaction (monitored by TLC, 100% EtOAc), the reaction mixture was quenched with 1N HCl at 0° C. temperature and extracted with EtOAc (2 mL×3). The combined organic layers were dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ: 13.24 (s, 1H), 9.18 (s, 1H), 8.45 (d, J=1.2 Hz, 1H), 7.80 (d, J=1.5, Hz, 1H), 7.53 (d, J=5.4 Hz, 2H), 7.41-7.34 (m, 2H), 5.24 (s, 2H), 1.38 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710043B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-ce3feacf23ca448096bb0c03a1f51644 |
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| Source note | uspto-grants-2014_04 |
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