HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384299Generated: October 31, 2026
Sodium Bicarbonate → HCID 178433829, compound
https://huagongshe.com/reaction/384299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acid | HCID 21072315 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 3-Methyl-1-(5,6,7,8-tetrahydronaphthalen-2-yl)-1H-pyrazol-5(4H)-one | HCID 51036580 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178433829 | HCID 178433829 | 13.1% |
Reaction Steps
Upon cooling by an ice-water bath, 3′-amino-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid 2f (250 mg, 1.01 mmol) was dissolved in 10 mL of hydrochloric acid (1 N) followed by addition of 10 mL of aqueous sodium nitrite (77 mg, 1.12 mmol) and 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 4i (230 mg, 1.01 mmol). The mixture was adjusted to pH 8 with saturated aqueous sodium bicarbonate, followed by addition of 10 mL of ethanol. The reaction was warmed up to room temperature overnight and monitored by TLC until the disappearance of the starting materials. The mixture was filtered, dried and recrystallized from methanol to obtain the title compound 5′-fluoro-2′-hydroxy-3′-{N′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthalen-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-biphenyl-3-carboxylic acid 4 (64 mg, yield 13.1%) as a red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367710B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-0767224f66574e67bd6d980515277809 |
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| Source note | uspto-grants-2013_02 |
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