HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641766Generated: October 31, 2026
Tert-butyldicarbonate → HCID 135510703, compound
https://huagongshe.com/reaction/641766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Reactant | HCID 135510683 | HCID 135510683 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135510703 | HCID 135510703 | 69.1% |
Reaction Steps
A mixture of 4-(6-chloro-2,3-methylenedioxyanilino)-7-hydroxy-5-piperidin-4-yloxyquinazoline (1.4 g), di-(tert-butyl dicarbonate (0.737 g) and DMF (14 ml) was stirred at ambient temperature for 2 hours. The mixture was evaporated and the residue was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using a 24:1 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound (1.2 g); NMR Spectrum: (CDCl3) 1.5 (s, 9H), 1.7-1.9 (m, 2H), 2.0-2.15 (m, 2H), 3.0-3.15 (m, 2H), 3.8-3.95 (m, 2H), 4.6 (m, 1H), 6.02 (s, 2H), 6.55 (s, 1H), 6.72 (d, 1H), 6.98 (m, 2H), 8.4 (s, 1H), 9.4 (s, 1H); Mass Spectrum: M+H+ 515 and 517.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696214B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-acce2966284246baba42ca1575b4aef1 |
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| Source note | uspto-grants-2010_04 |
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