Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 86701395 | HCID 86701395 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86701396 | HCID 86701396 | 81% |
Reaction Steps
BCl3 (1 M in CH2Cl2, 9.0 mL, 9.0 mmol) was added dropwise to a solution of (2S,5R)-6-(benzyloxy)-2-(1,3,4-thiadiazol-2-yl)-1,6-diaza-bicyclo[3.2.1]octan-7-one (560 mg, 1.8 mmol) in dry CH2Cl2 (20 mL) at −78° C. The mixture was stirred under a N2 atmosphere at 0° C. for 6 hrs., then, MeOH (9 mL) was slowly added dropwise at −78° C. The solvents were evaporated under vacuum at 0° C. to give (2S,5R)-6-hydroxy-2-(1,3,4-thiadiazol-2-yl)-1,6-diaza-bicyclo[3.2.1]octan-7-one (329 mg, 81%) as a yellow solid, which was used directly in the next step. ESI-MS (EI+, m/z): 227.1 [M+H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969570B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a9e5c256112444e9b98f891f1ad3f6eb |
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| Source note | uspto-grants-2015_03 |
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