Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 59331324 | HCID 59331324 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59331256 | HCID 59331256 | 75% |
Reaction Steps
To a solution of [6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]acetic acid (0.320 g) in N,N-dimethylformamide (6 mL) were added 1-hydroxybenzotriazole ammonia complex (234 mg), triethylamine (0.271 mL) and N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (186 mg), and the mixture was stirred at room temperature for 16 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated, under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:hexane=50:50-100:0, volume ratio) and recrystallized from hexane-acetone to give the title compound (0.240 g, yield 75%) as colorless crystals. MS: 494 (MH+). melting point 151-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318746B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-b4749419f9f741699f5cfdd02eccc245 |
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| Source note | uspto-grants-2012_11 |
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