HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180138Generated: October 31, 2026
Triphenylphosphine → HCID 22490029, compound
https://huagongshe.com/reaction/2180138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 21936040 | HCID 21936040 | — |
| Reactant | 4-(4-Fluoro-2-methylindol-5-yloxy)-7-hydroxy-6-methoxycinnoline | HCID 135749776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22490029 | HCID 22490029 | 24% |
Reaction Steps
Diethyl azodicarboxylate (0.095 ml, 0.6 mmol) was added dropwise to a suspension of 4-(4-fluoro-2-methylindol-5-yloxy)-7-hydroxy-6-methoxycinnoline (0.1 g, 0.3 mmol), prepared as described in Example 4), 3-(4-cyanomethylpiperazin-1-yl)propan-1-ol (0.085 g, 0.45 mmol) and triphenylphosphine (0.155 g, 0.6 mmol) in methylene chloride (2.5 ml). The mixture was stirred for 30 minutes at ambient temperature. Further 3-(4-cyanomethylpiperazin-1-yl)propan-1-ol (0.085 g, 0.45 mmol), triphenylphosphine (0.155 g, 0.6 mmol) and diethyl azodicarboxylate (0.095 ml, 0.6 mmol) were added. The mixture was stirred for 30 minutes and the volatiles were removed under vacuum. The residue was purified by column chromatography eluting with ethylacetate/methylene chloride (1/1) followed by methanol/ethyl acetate/methylene chloride (5/45/50 followed by 10/40/50 and 10/0/90). The fractions containing the expected product were combined and evaporated to give 7-(3-(4-cyanomethylpiperazin-1-yl)propoxy)-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnoline (0.035 g, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06887874B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-44d2369bd853456186b8f7a6a2b30f81 |
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| Source note | uspto-grants-2005_05 |
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