HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384322Generated: October 31, 2026
Sodium Bicarbonate → HCID 178433806, compound
https://huagongshe.com/reaction/384322
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 3-Methyl-1-(5,6,7,8-tetrahydronaphthalen-2-yl)-1H-pyrazol-5(4H)-one | HCID 51036580 | — |
| Reactant | HCID 178479035 | HCID 178479035 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178433806 | HCID 178433806 | 34.9% |
Reaction Steps
3-Amino-3′-(1H-tetrazol-5-yl)-biphenyl-2-ol hydrochloride 8f (340 mg, 1.34 mmol) was dissolved in 3 mL of 1 N hydrochloric acid followed by dropwise addition of 3 mL of aqueous sodium nitrite (98 mg, 1.41 mmol) upon cooling by an ice-water bath. After the mixture was reacted for 10 minutes, 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 3i (276 mg, 1.21 mmol), sodium bicarbonate (1.69 g, 20 mmol) and 3 mL of ethanol were added successively. The reaction mixture was reacted at room temperature for 18 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was washed with 20 mL of water and then dissolved in 20 mL of water. Upon cooling by an ice-water bath, the mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid. Then the mixture was filtered and dried to obtain the title compound 4-{[2-hydroxy-3′-(1H-tetrazol-5-yl)-biphenyl-3-yl]-hydrazono}-5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 10 (208 mg, 31.6%) as a yellow 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-aa1cf1dba57c449998248a0875695af4 |
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| Source note | uspto-grants-2013_02 |
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