HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → HCID 24948587, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86617456 | HCID 86617456 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24948587 | HCID 24948587 | 55% |
Reaction Steps
To a solution of morpholine (0.050 mL, 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 (85 mg, 55%). 1H NMR (DMSO-d6) δ 8.35 (1H), 8.05 (1H), 7.08 (1H), 6.85 (1H), 3.65 (4H), 4.05 (4H), 3.53 (4H), 3.18 (2H), 2.75 (2H), 2.45 (4H); m/z (M+H)=345.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501438B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-62535478035b4277b4d3fd555068c463 |
| Source note | uspto-grants-2009_03 |