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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271876Generated: November 1, 2026

tert-butyl N-(2-oxoethyl)carbamate → HCID 9932869, compound

https://huagongshe.com/reaction/1271876

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(2-oxoethyl)carbamateHCID 4247255—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 18455022HCID 18455022—
Reactant2-(1-amino-2-methylpropyl)-3-benzyl-7-chloroquinazolin-4(3H)-oneHCID 22238798—
SolventDichloromethaneHCID 6344—
ProductHCID 9932869HCID 9932869—

Reaction Steps

Preparation of {2-[1-(3-Benzyl-7-chloro-4-oxo-3,4-dihydro-quinazolin-2-yl)-2-methyl-propylamino]-ethyl}-carbamic acid tert-butyl ester: Sodium triacetoxyborohydride (172 mg, 0.81 mmol) was added to a solution containing 2-(1-amino-2-methyl-propyl)-3-benzyl-7-chloro-3H-quinazolin-4-one (185 mg, 0.54 mmol) (prepared using the general procedure described in WO 0130768) and tert-butyl N-(2-oxoethyl)carbamate (103 mg, 0.65 mmol) in CH2Cl2 (5.4 mL). The resulting mixture was stirred at room temperature overnight. The reaction was diluted with CH2Cl2 (10 mL), washed with brine, dried and concentrated under vacuum. Purification by flash chromatography on silica gel (5–10% EtOAc in hexane) gave the title compound (105 mg) as a white solid: MS (ES) m/e 485 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208487B2
Source datasetuspto-grants-2007_04
ORD IDord-379cbff2e277442fa796ec9369a063c8
Source noteuspto-grants-2007_04