HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640995Generated: October 29, 2026
Tetrahydrofuran → HCID 178426949, compound
https://huagongshe.com/reaction/640995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Aminobenzyl alcohol | HCID 69331 | — |
| Reactant | HCID 178426964 | HCID 178426964 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178426949 | HCID 178426949 | 24% |
Reaction Steps
A small screw cap test tube was charged with 2,5-Dimethyl-2H-pyrazole-3-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 60, 300 mg, 0.746 mmol) and THF (7.5 mL). To the resulting solution was added (4-amino-phenyl)-methanol (133 mg, 0.955 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and the resulting suspension was filtered. The solids collected were washed with 0° C. iPrOH (5 mL) and set aside. The filtrate was concentrated in vacuo and the residue obtained was dissolved in EtOAc (5 mL). The resulting solution was triturated with Hexanes (˜50 mL) to yield a precipitate. This precipitate was then filtered and washed with 0° C. iPrOH (5 mL). The solids collected were combined with those previously set aside to afford the title compound in 24% yield (0.091 g, 0.179 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07692005B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d579bc6379384c1390635c0cf1601b06 |
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| Source note | uspto-grants-2010_04 |
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