Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 71090374 | HCID 71090374 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71090272 | HCID 71090272 | 167.5% |
Reaction Steps
To a solution of (2R)-2-amino-N-[6-[(3,3-dimethyl-1H-isobenzofuran-5-yl)oxy]-3-pyridyl]butanamide (Intermediate 61, 18 mg, 0.0527 mmol) in DCM (4 mL) N,N-diethylethanamine (0.022 ml, 0.16 mmol) was added and the reaction mixture was cooled to 0° C. A solution of bis(trichloromethyl) carbonate (7.8 mg, 0.026 mmol) in DCM (1 mL) was slowly added and the reaction mixture was stirred for 30 minutes at the same temperature. The reaction was diluted with DCM (5 ml) and washed with an aqueous saturated solution of NH4Cl (10 ml). The organic layer was dried (Na2SO4), filtered and evaporated and the residue was purified by flash chromatography (Biotage system) on silica gel using a SNAP 10 g as column and cyclohexane/ethyl acetate from 80:20 to 10:90 as eluent affording the title compound (16 mg) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193704B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-d17d9aa9aad24873851d4f1e3b76ea39 |
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| Source note | uspto-grants-2015_11 |
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