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 67132862 | HCID 67132862 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67132972 | HCID 67132972 | 70% |
Reaction Steps
To a solution of 3-(3-imidazo[4,5-b]pyridin-3-ylmethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (53.6 mg, 0.111 mmol; see Example 8(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 (32.9 mg, 0.222 mmol) and butyl chloroformate (141.3 μL, 1.11 mmol) and the reaction mixture was stirred overnight. Citric acid (3 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 purified by LCMS (20-100% CH3CN in water) to give the title compound in 70% yield, over two steps, (41 mg, 0.078 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-b7940f79ea144a8382c06969526072e1 |
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| Source note | uspto-grants-2011_12 |
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