HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241574Generated: October 30, 2026
Triphenylphosphine → HCID 21936093, compound
https://huagongshe.com/reaction/1241574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Pyrrolidineethanol | HCID 76288 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 135594114 | HCID 135594114 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21936093 | HCID 21936093 | 12.9% |
Reaction Steps
Diethyl azodicarboxylate (0.182 ml) was added dropwise to a stirred mixture of 4-(6-chloro-2,3-methylenedioxyanilino)-7-hydroxy-6-methoxyquinazoline (0.2 g), N-(2-hydroxyethyl)pyrrolidine (0.086 g), triphenylphosphine (0.303 g) and methylene chloride (3 ml) and the reaction mixture was stirred at ambient temperature for 15 minutes. The reaction mixture was evaporated and the residue was purified by column chromatography on silica using a 45:4:1 mixture of methylene chloride, methanol and a saturated methanolic ammonia solution as eluent. There was thus obtained the title compound (0.033 g) as a white solid; NMR Spectrum: (DMSOd6 and CF3CO2D) 1.9 (m, 2H), 2.1 (m, 2H), 3.2 (m, 2H), 3.7 (m, 2H), 3.8 (m, 2H), 4.05 (s, 3H), 4.6 (m, 2H),6.2 (s, 2H), 7.1 (d, 1H), 7.5 (s, 1H), 8.2 (s, 1H), 8.95 (s, 1H); Mass Spectrum: M−H− 441 and 443.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115615B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-5d84eb2fe9b04c2dbbcea67c2db48ea4 |
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| Source note | uspto-grants-2006_10 |
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