HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454101Generated: October 29, 2026
Triphenylphosphine → 7-(3-(Ethylsulphonyl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline
https://huagongshe.com/reaction/454101
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-(Ethanesulfonyl)propan-1-ol | HCID 12943303 | — |
| Reactant | 7-hydroxy-6-methoxy-4-(2-methyl-1H-indol-5-yloxy)quinazoline | HCID 135763108 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(3-(Ethylsulphonyl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline | HCID 22030568 | 55.2% |
Reaction Steps
Diethyl azodicarboxylate (117 mg, 0.67 mmol) was added in portions to a solution of 7-hydroxy-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (120 mg, 0.37 mmol), (prepared as described in Example 49), and 3-(ethylsulphonyl)-1-propanol (74 mg, 0.48 mmol) in methylene chloride (3.5 ml) and triphenylphosphine (176 mg, 0.67 mmol). After stirring for 2 hours at ambient temperature, the residue was poured onto a column of silica and eluted with ethyl acetate/methylene chloride (1/1) followed by methylene chloride/methanol (97/3 followed by 95/5). After removal of the solvent under vacuum, the residue was triturated with ether, filtered and dried under vacuum to give 7-(3-(ethylsulphonyl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (93 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492560B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-4c91bd87dc084929b8cc975b4d987d61 |
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| Source note | uspto-grants-2013_07 |
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