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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641766Generated: October 31, 2026

Tert-butyldicarbonate → HCID 135510703, compound

https://huagongshe.com/reaction/641766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyldicarbonateHCID 22064466—
ReactantHCID 135510683HCID 135510683—
SolventDimethylformamideHCID 6228—
ProductHCID 135510703HCID 13551070369.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696214B2
Source datasetuspto-grants-2010_04
ORD IDord-acce2966284246baba42ca1575b4aef1
Source noteuspto-grants-2010_04