HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426282Generated: November 1, 2026
S-2-naphthylmethyl thioacetimidate → HCID 178465558, compound
https://huagongshe.com/reaction/2426282
Participants
| Role | Name | HCID | Charge |
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| Reactant | S-2-naphthylmethyl thioacetimidate | HCID 10856874 | — |
| Reactant | 6-Amino-2-(3,4-methylendioxy-phenyl)quinazoline | HCID 44140427 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178465558 | HCID 178465558 | 42% |
Reaction Steps
A suspension in ethanol (80 ml) of 6-amino-2-(3,4-methylendi-oxy-phenyl)-quinazoline (5 g, 0.019 mol) and S-2-naphthylmethyl thioacetimidate bromidrate (5.63 g, 0.019 mol, prepared as described in Tetrahedron Letters 38, 179-182 (1997), was stirred at r.t. for 24 hrs. Then S-2-naphthylmethyl thioacetimidate bromidrate (2.8 g, 0.010 mol) was added and the mixture was stirred at r.t. for further 24 hrs., then was concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The aqueous layer was basified with Na2CO3 and extracted with ethyl acetate. The product was extracted with aqueous HCl (0.001 N) for three times. The aqueous layers were collected, basified with Na2CO3 and extracted with ethyl acetate. The organic layer was washed with water and dried over Na2SO4, concentrated under reduced pressure, and then the residue was triturated with diethyl ether. The yellow solid was filtered and dried in vacuum to give the titled product (2.4 g, 42% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968558B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-27d787c1f59842f882124675e3d846e4 |
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| Source note | uspto-grants-2011_06 |
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