HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503554Generated: October 30, 2026
1-Chloro-4-phenylphthalazine → HCID 59427310, compound
https://huagongshe.com/reaction/503554
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-4-phenylphthalazine | HCID 272109 | — |
| Reactant | HCID 67317411 | HCID 67317411 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 59427310 | HCID 59427310 | — |
Reaction Steps
A 5 ml microwave tube was charged with 7-(4-aminophenoxy)thieno[3,2-b]pyridine-2-carboxamide (85 mg, 0.300 mmol) and 1-chloro-4-phenylphthalazine (60 mg, 0.250 mmol) in 2.0 ml of tert-butanol. The vessel was capped and irradiated at 140° C. for 15 minutes in the microwave. Analysis of an aliquot of the crude mixture by LCMS showed remaining starting material and approximately 20% conversion to desired product. Irradiated at 150° C. for an additional 20 minutes, at which time reaction was deemed complete by LCMS analysis. Cooled to ambient temperature and diluted reaction mixture with methanol. Filtered solids, washed with additional methanol and concentrated in vacuo to afford 7-(4-(4-phenylphthalazin-1-ylamino)phenoxy)thieno[3,2-b]pyridine-2-carboxamide. MS m/z=490 [M+H]+. Calc'd for C28H19N5O2S: 489.55.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776857B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c5006ff782b649b3bca3d225e1285484 |
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| Source note | uspto-grants-2010_08 |
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