Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diethyl (1S,2S,5R,6S)-2-benzyloxycarbonylamino-4-methylene-bicyclo[3.1.0]hexane-2,6-dicarboxylate | HCID 86691272 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 86691273 | HCID 86691273 | 106.1% |
Reaction Steps
To a jacketed reaction flask connected to a chiller unit, add diethylzinc solution (157.2 mL, 157.2 mmol, 1M in heptanes) under a nitrogen atmosphere. Cool the solution to −15° C. and dilute with cold (−15° C.), dry dichloroethane (157.2 mL). Dissolve trifluoroacetic acid (11.1 mL, 146.7 mmol) in dichloroethane (11.1 mL) and add to the reaction vessel over 50 minutes, keeping the internal temperature below −10° C. Stir the resulting suspension at −10 to −15° C. for 30 minutes. Dissolve diiodomethane (12.7 mL, 42.1 g, 157.2 mmol) in dichloroethane (12.7 mL) and add to the reaction mixture over 50 minutes, keeping the internal temperature below −10° C. Stir the resulting thin, white suspension at −10 to −15° C. for 30 minutes. Dissolve diethyl (1S,2S,5R,6S)-2-benzyloxycarbonylamino-4-methylene-bicyclo[3.1.0]hexane-2,6-dicarboxylate (20.3 g, 87.9% potency, 46.0 mmol) in dichloroethane (30.4 mL) and add to the reaction mixture over 10 minutes, keeping the internal temperature below −10° C. Stir the clear, pale yellow solution at −10° C. for 5 minutes and monitor for latent exotherms. Change the set point on the chiller to 0° C. and stir the reaction mixture at that temperature for 48 hours. Quench the reaction mixture by addition of 5N HCl (62.9 mL, 314.4 mmol) over 15 minutes, keeping the internal temperature below 6° C. Stir the resulting mixture at 0-5° C. for 20 minutes, then transfer to a funnel and separate the layers. Wash the organic layer with 1N HCl (2×50 mL) followed by 1:1 saturated NaHCO3/H2O (60 mL), 1:1 saturated Na2CO3/H2O (60 mL) and water (50 mL). Dry the organics over Na2SO4 and concentrate in vacuo to afford the title compound as a pale yellow oil (19.6 g, 60.3% potent, 63.9% corrected yield). 1H NMR (DMSO-d6) δ 0.37 (m, 2H), 0.52-0.55 (dm, 2H), 1.13-1.17 (m, 6H), 1.49-1.50 (m, 1H), 1.51-1.56 (m, 1H), 1.60-1.79 (m, 2H), 3.97-4.10 (m, 5H), 5.00 (s, 2H), 7.29-7.34 (m, 5H), 8.04 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575214B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-a555521eb23147408decbd6ca84cbaca |
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| Source note | uspto-grants-2013_11 |
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