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 67133102 | HCID 67133102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67133142 | HCID 67133142 | 73% |
Reaction Steps
To a solution of 3-[3-(2-ethylimidazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (55.1 mg, 0.120 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, concentrated in vacuo. To the crude product dissolved in pyridine (1.5 mL) was added pyrrolidinopyridine (35.5 mg, 0.240 mmol) and butyl chloroformate (152.5 μL, 1.20 mmol) and the reaction mixture was stirred overnight. Citric acid (3 mL, 10% aq) was added to the reaction mixture, extracted with EtOAc, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue was purified by flash chromatography using MeOH:CH2Cl2 (5:95 to 8:92) as eluent to give the title compound in 73% yield, over two steps, (44.3 mg, 0.088 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-e06a0e86177541f2b5464cb2de5ccf6d |
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| Source note | uspto-grants-2011_12 |
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