Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Propanethiol | HCID 6364 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13319603 | HCID 13319603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21246126 | HCID 21246126 | — |
Reaction Steps
A solution of benzyl 6-(1-hydroxyethyl)-3-chloro-1-azabicyclo[3.2.0]hept-2-ene-7-one-2-carboxylate (32 mg) in anhydrous dimethylformamide (DMF, 2 ml) is cooled to -40° C. and stirred under a nitrogen atmosphere. A solution of isopropylmercaptan (8 mg) in anhydrous DMF (1 ml) containing 57% sodium hydride (4.4 mg) is added dropwise over 10 mins. The resulting solution is stirred for 2 hrs, with gradual warming to 0° C. The solution is diluted with ethyl acetate (20 ml), washed with water (5×10 ml) and brine, dried over MgSO4, filtered, and evaporated in vacuo. The residue is purified by plc on silica gel GF to yield benzyl 6-(1-hydroxyethyl)-3-isopropylthio-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820817 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-a2a5214eee1a4bc1834859e9f5a1d29f |
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| Source note | uspto-grants-1989_04 |
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