HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405110Generated: October 31, 2026
3-Chloro-6-fluorobenzo[b]thiophene-2-carbonyl chloride → 3-((4-(3-chloro-6-fluorobenzo[b]thiophene-2-carboxamido)phenyl)amino)-5-((4-hydroxybenzyl)amino)-1H-pyrazole-4-carboxamide
https://huagongshe.com/reaction/1405110
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-6-fluorobenzo[b]thiophene-2-carbonyl chloride | HCID 2783173 | — |
| Reactant | HCID 178513736 | HCID 178513736 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-((4-(3-chloro-6-fluorobenzo[b]thiophene-2-carboxamido)phenyl)amino)-5-((4-hydroxybenzyl)amino)-1H-pyrazole-4-carboxamide | HCID 178513737 | 6% |
Reaction Steps
3-((4-aminophenyl)amino)-5-((4-hydroxybenzyl)amino)-1H-pyrazole-4-carboxamide (100 mg) was dissolved in 3.0 mL of DMF and TEA (125 μL, 3.0 eq.) was then added to the reaction vessel. Reaction was then stirred on an ice bath for 15 min and 3-Chloro-6-fluorobenzo[b]thiophene-2-carbonyl chloride (75 mg, 1.00 eq.) dissolved in DMF (2.0 mL) was slowly added into the reaction. The reaction continued stirring for 18 hrs and allowed to reach room temperature. The reaction was tracked via HPLC, once completed and no traces of starting material is present, the solvent was then removed via vacuo and column chromatography was used to purify the compound. A gradient of 0 to 20% MeOH in dichloromethane was used and the desired fractions were combined, evaporated and triturated with diisoproyl ether then filtered to yield product as an off white powder (0.008 g, 6.0% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916555B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-f22fbf7666be47f89114523708e4ca55 |
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| Source note | uspto-grants-2014_12 |
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