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
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl N-(2-oxoethyl)carbamate | HCID 4247255 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 18455022 | HCID 18455022 | — |
| Reactant | 2-(1-amino-2-methylpropyl)-3-benzyl-7-chloroquinazolin-4(3H)-one | HCID 22238798 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9932869 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208487B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-379cbff2e277442fa796ec9369a063c8 |
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| Source note | uspto-grants-2007_04 |
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