HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924460Generated: October 30, 2026
1-Methylpiperazine → 3-{[(Benzyloxy)carbonyl]amino}-7-(4-methylpiperazin-1-yl)quinoline-2-carboxylic acid
https://huagongshe.com/reaction/924460
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl | HCID 16217985 | — |
| Reactant | Ethyl 3-(((benzyloxy)carbonyl)amino)-7-bromoquinoline-2-carboxylate | HCID 86726857 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-{[(Benzyloxy)carbonyl]amino}-7-(4-methylpiperazin-1-yl)quinoline-2-carboxylic acid | HCID 86726904 | — |
Reaction Steps
A mixture of ethyl 3-{[(benzyloxy)carbonyl]amino}-7-bromoquinoline-2-carboxylate (300 mg, 0.7 mmol), 1-methylpiperazine (200 mg, 2 mmol), Pd(OAc)2 (20 mg), dicyclohexyl(2′,6′-diisopropoxybiphenyl-2-yl)phosphine (49 mg, 0.10 mmol), and K3PO4 (580 mg, 2.8 mmol) in tert-butyl alcohol (10 mL) was purged with N2 prior and then heated at 100° C. in a sealed vial for 2 h. The mixture was allowed to cool, diluted with EtOAc, and then filtered through a diatomaceous earth plug. The filtrate was concentrated under reduced pressure. To the resulting residue, 10 mL of dioxane and 4 mL of 2.5 M NaOH were added.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278950B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-1689f88c606d4e27b3ed67ca12a49fb3 |
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| Source note | uspto-grants-2016_03 |
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