HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83988Generated: October 26, 2026
4-Chloroquinazolin-6-yl acetate → (R)-4-(1-phenylethylamino)quinazolin-6-yl acetate
https://huagongshe.com/reaction/83988
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloroquinazolin-6-yl acetate | HCID 18967624 | — |
| Reactant | (R)-1-(3-Chloro-4-fluorophenyl)ethanamine | HCID 28602988 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (R)-4-(1-phenylethylamino)quinazolin-6-yl acetate | HCID 66755670 | 89.7% |
| Product | (R)-4-(1-Phenylethylamino)quinazolin-6-ol | HCID 66756048 | — |
Reaction Steps
A mixture of compound 0204 (1.0 g, 4.5 mmol) and (R)-1-(3-chloro-4-fluoro-phenyl)ethanamine (0.87 g, 5.0 mmol) in isopropanol (45 mL) was stirred at 90° C. for 1 hour. The mixture was cooled to room temperature and the resulting precipitate was isolated. The solid was washed in turn with isopropanol and methanol, dried to provide the title compound (R)-4-(1-phenylethylamino)quinazolin-6-yl acetate as a yellow solid (0.62 g, 61%): LCMS 308 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846912B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-08feaa61083e4e36800ab32b8c74f444 |
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| Source note | uspto-grants-2014_09 |
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