Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 66578955 | HCID 66578955 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66580618 | HCID 66580618 | — |
Reaction Steps
Enantiomer A of 1- [1-(2-chloroethyl)piperidin-3-yl]-3-(morpholin-4-ylcarbonyl)-1,4-dihydrothiochromeno[4,3-c]pyrazole 5,5-dioxide (274 mg; 0.57 mmol; 1.00 eq.), morpholine (199 μl; 2.29 mmol; 4.00 eq.), sodium iodide (85 mg; 0.57 mmol; 1.00 eq.) and K2CO3 (237 mg; 1.72 mmol; 3.00 eq.) are taken up in ACN (6 mL). The reaction mixture is stirred at 60° C. overnight. The reaction mixture is diluted in DCM and washed with water, brine, then dried over MgSO4 and evaporated. Purification by flash chromatography (DCM/MeOH 0 to 5%) followed by dissolution in ACN : water and freeze drying gives the title compound as a white solid. 1H NMR (DMSO-d6, 300 MHz): δ 8.05 (dd, J =1.2, 7.8 Hz, 1H), 7.94 (td, J =1.3, 7.8 Hz, 1H), 7.88-7.81 (m, 11-1), 7.80-7.70 (m, 1H), 5.05-4.62 (m, 3H), 4.05-3.79 (m, 2H), 3.79-3.58 (m, 6H), 3.56-3.42 (m, 4H), 3.32-3.08 (m, 3I-1), 2.91 (d, J =10.8 Hz, 1H), 2.46-2.22 (m, 8H), 2.20-1.60 (m, 6H). MS (ESI+): 530.46. HPLC (max plot) 99.4%; Rt 1.56 min. [α]25D+4.20 (c 1.09, DCM).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073940B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-b81e6d4a0e444e729d2d607fef192f84 |
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| Source note | uspto-grants-2015_07 |
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