Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Naphthylamine | HCID 8640 | — |
| Reactant | HCID 86617456 | HCID 86617456 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24948782 | HCID 24948782 | 32.2% |
Reaction Steps
To a solution of 1-naphylamine (0.077 g, 0.54 mmol) and triethylamine (0.16 mL, 1.14 mmol) in CH2Cl2 (10 mL) was added 3-(2-morpholin-4-yl-ethyl)-imidazo[1,5-a]pyridine-1-carbonyl chloride hydrochloride (150 mg, 0.45 mmol). The mixture was stirred at ambient temperature for 1 h then washed with sat. aq. NaHCO3 (20 mL). The organic layer was separated and the aqueous layer was extracted with dichloromethane (20 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was chromatographed on silica to yield the title compound (58 mg, 32%). 1H NMR (DMSO-d6) δ 10.0 (1H), 8.45 (1H), 8.10 (1H), 7.98 (3H), 7.78 (1H), 7.55 (3H), 7.18 (1H), 6.93 (1H), 3.59 (4H), 3.30 (2H), 2.85 (2H), 2.57 (4H); m/z (M+H)=401.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501438B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-0d66ee03b78c44c5bb4aabb7d442f349 |
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| Source note | uspto-grants-2009_03 |
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