Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | HCID 18401525 | HCID 18401525 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9953707 | HCID 9953707 | — |
Reaction Steps
To a stirred suspension of 4-N-acetylsulphanilyl chloride (2.7 g, 11.55 mmol) and triethylamine (1.95 g, 19.25 mmol) in dichloromethane (50 ml) was added portionwise solid 3,6-dihydro-3,5-dimethyl-6-(4-methoxyphenyl)-2H-1,2-oxazine hydrochloride (1.97 g, 7.70 mmol). The resulting solution was stirred at room temperature for 5 h then washed with water three times, aqueous sodium hydroxide (2M), water and brine. The organic phase was dried over magnesium sulphate, filtered and evaporated, the resulting foam was purified on flash silica eluting with ethylacetate-hexane (3:2) to give 2-(4-acetamidobenzenesulphonyl)-3,6-dihydro-3,5-dimethyl-6-(4-methoxyphenyl)-2H-1,2-oxazine as a white foam. 1H NMR (CDCl3) δ 1.39(3H,s), 1.41(3H, d), 2.20(3H, s), 3.79(3H, s), 4.45(1H, m), 5.19(1H, s), 5.68(1H, d), 6.80(2H, d), 7.13(2H, d), 7.57(1H, bs), 7.59(2H, d), 7.80(2H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482824B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-06e647e335804ae781fc6380e814ac72 |
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| Source note | uspto-grants-2002_11 |
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