Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Reactant | 2-(Pyrrolidin-1-yl)pyridine | HCID 11019020 | — |
| Reactant | HCID 67133186 | HCID 67133186 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67133104 | HCID 67133104 | 69% |
Reaction Steps
To a solution of 3-(3-pyrazol-1-ylmethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (82.4 mg, 0.191 mmol; see step (a)) in CH2Cl2 (2 mL) was added BCl3 (0.6 mL, 1.0 M in hexane) and the reaction mixture was stirred for 1 h at ambient temperature. The reaction mixture was concentrated in vacuo. Water (5 mL) was added to the residue and this was then extracted with EtOAc. The combined organic phase was washed with water and brine, dried (over anhydrous MgSO4) and concentrated in vacuo. To the crude product dissolved in pyridine (1.5 mL) was added pyrrolidinopyridine (42.7 mg, 0.288 mmol) and butyl chloroformate (192.6 μL, 1.91 mmol) and the reaction mixture was stirred overnight. Citric acid (5 mL, 10% aq) was added to the reaction mixture, which was then extracted with EtOAc, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue was purified by LCMS (30-100% CH3CN in water) to give the title compound in 69% yield, over two steps, (62.7 mg, 0.132 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080571B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-ad6af54bcfe84af4918b0c3dab0ab493 |
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| Source note | uspto-grants-2011_12 |
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