Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 22276535 | HCID 22276535 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22277046 | HCID 22277046 | — |
Reaction Steps
To a solution of tert-butyl 2-[4-tert-butoxycarbonyl-7-(5-(4-(5-oxazolyl)phenyl)-2-thienyl)-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetate (4.7 g) in ethyl acetate (40 ml) was added dropwise a solution 4N-hydrogen chloride in ethyl acetate (40 ml) under ice-cooling. After being stirred at 0° C. for 30 minutes and at ambient temperature for 1 hour, reaction mixture was concentrated in vacuo and hydrogen chloride was azeotropically removed with toluene to give tert-butyl 2-[7-(5-(4-(5-oxazolyl)phenyl)-2-thienyl)-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetate hydrochloride (4.2 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06967197B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-4ed15cd16ad448fca8a63f2867d235b3 |
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| Source note | uspto-grants-2005_11 |
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