HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893687Generated: October 31, 2026
Hydrazine hydrate (1:1) → HCID 178487706, compound
https://huagongshe.com/reaction/1893687
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 178498512 | HCID 178498512 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178487706 | HCID 178487706 | 80% |
Reaction Steps
To a solution of 4-hydroxy-7-methoxy-quinoline-2-carboxylic acid methyl ester (2.0 g, 8.58 mmol) in methanol (85 mL) was added hydrazine mono hydrate (1.7 g, 34.3 mmol) and the mixture was refluxed for 6 hours. The crude reaction mixture was concentrated in vacuo and the residue was taken up in methanol and poured onto an ice/water mixture (800 mL). A white precipitate formed, which was collected by filtration and washed with cold water. The filter cake was then dried on house vacuum by passing air through in sintered glass funnel, and then dried on vacuum oven at 45° C. overnight to afford 4-hydroxy-7-methoxy-quinoline-2-carboxylic acid hydrazide (1.6 g, 80% yield). 1H NMR (DMSO-d6, 300 MHz) δ 11.57 (s, 1H), 10.28 (s, 1H), 7.95 (d, 1H), 7.43 (d, 1H), 7.01-6.91 (m, 1H), 6.54 (s, 1H), 4.72 (br s, 2H), 3.82 (s, 3H). LCMS found 234.18 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513186B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-35db02cbe6a845f89a445744f8758de3 |
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| Source note | uspto-grants-2013_08 |
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