Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | HCID 86673873 | HCID 86673873 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68283781 | HCID 68283781 | — |
Reaction Steps
Methanesulfonic acid 2-(1-carbamoyl-3-{2-[(1R,3S,5R)-3-(3-chloro-2-fluoro-benzylcarbamoyl)-2-aza-bicyclo[3.1.0]hex-2-yl]-2-oxo-ethyl}-1H-indol-5-yloxy)-ethyl ester in a solution of dimethylamine 5.6 M in EtOH (1 mL) was sealed in a microwave vial and heated at 70° C. for 2 h (Emrys Optimizer; personal chemistry). The reaction mixture was quenched by addition of saturated aqueous NaHCO3, extracted with EtOAc, dried (Na2SO4) and evaporated in vacuo. Then crude residue was purified by catch-release (SCX Tosic Acid-1 g from Silicycle; eluent MeOH (10 mL) to 2M ammonia in MeOH (10 mL)) to give the desired material which was precipitated in Et2O. MS (UPLC/MS): 556.5/558.5 [M+H]+, 600.4/602.5 [M+HCOO]−; tR (HPLC conditions f): 1.46 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085555B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-7e7deef0716848378c64a819e8d9cd49 |
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| Source note | uspto-grants-2015_07 |
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