HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238717Generated: October 31, 2026
Sodium Bicarbonate → HCID 178433799, compound
https://huagongshe.com/reaction/238717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 2-Indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one | HCID 57483780 | — |
| Reactant | 4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide | HCID 57483846 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178433799 | HCID 178433799 | 28.7% |
Reaction Steps
4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 19c (120 mg, 0.38 mmol) was dissolved in 2.7 mL of 1 M hydrochloric acid upon cooling by an ice-water bath, followed by dropwise addition of 0.45 mL of sodium nitrite solution (29 mg, 0.42 mmol). After the mixture was reacted for 20 minutes, 2-indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one 1i (73 mg, 0.34 mmol) was added. The mixture was adjusted to pH 8 with saturated sodium bicarbonate solution followed by addition of 2 mL of ethanol. The reaction mixture was reacted overnight at room temperature. The mixture was filtered and the filter cake was added to 20 mL of water. The mixture was adjusted to pH 3-4 with concentrated hydrochloric acid and filtered. Then 5 mL of ethyl acetate was added to the filter cake and the mixture was stirred for 1 hour. The mixture was filtered and the filter cake was dried to obtain the title compound (Z)-4-{2-hydroxy-3-[N′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-phenyl}-thiophene-2-carboxylic acid 19d (45 mg, yield 28.7%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08642637B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-b82339e10f67415683af5fd9ac5ee238 |
|---|
| Source note | uspto-grants-2014_02 |
|---|