HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916477Generated: October 29, 2026
Triphenylphosphine → HCID 86597574, compound
https://huagongshe.com/reaction/916477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3-[4-(2-Fluoroethyl)piperazin-1-YL]propan-1-OL | HCID 45115767 | — |
| Reactant | 4-Chloro-6-methoxyquinazolin-7-ol | HCID 135742251 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86597574 | HCID 86597574 | 57% |
Reaction Steps
A suspension of 4-chloro-7-hydroxy-6-methoxyquinazoline (202 mg, 0.96 mmol), (prepared as described for the starting material in Example 4), in methylene chloride (10 ml) was treated with triphenylphosphine (352 mg, 1.35 mmol), 3-[4-(2-fluoroethyl)piperazin-1-yl)propan-1-ol (200 mg, 1.06 mmol), (prepared as described for the starting material in Example 27), and diisopropyl azodicarboxylate (226 mg, 1.15 mmol) and the mixture stirred at ambient temperature for 2 hours. The crude reaction mixture was loaded onto a silica column and eluted using methylene chloride/methanol (95/5). The relevant fractions were combined and evaporated under vacuum to give 4-chloro-7-{3-[4-(2-fluoroethyl)piperazin-1-yl]propoxy}-6-methoxyquinazoline (208 mg, 57%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268230B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-1a648fd298834a4f8062525c758a2048 |
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| Source note | uspto-grants-2007_09 |
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