HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713230Generated: November 4, 2026
Isopropylamine → HCID 118159347, compound
https://huagongshe.com/reaction/713230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,3-Dichloropyrido[3,4-b]pyrazine | HCID 23122731 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118159347 | HCID 118159347 | 65.7% |
Reaction Steps
To a solution of 2,3-dichloropyrido[3,4-b]pyrazine (2.5 g, 12.50 mmol) and DIPEA (6.53 mL, 37.5 mmol) in DCM (25 mL) was added propan-2-amine (1.065 mL, 12.50 mmol) at 0° C. The mixture was stirred at 0° C. for 30 min, warmed slowly to 23° C., and stirred for 12 h. The crude mixture was partitioned between EtOAc (100 mL) and saturated aqueous NH4Cl (100 mL). The layers were separated and the aqueous phase was washed with EtOAc (4×100 mL). The organic extracts were combined, washed with brine (50 mL), dried over Na2SO4, filtered, rinsed with EtOAc, and dried in vacuo. The crude material was dissolved in toluene (5 mL) and purified via medium pressure chromatography using a gradient eluant of 50% to 75% EtOAc in heptane on a 80 g silica gel column (Single Step™) to give the title compound (1.828 g, 65.7%) as a yellow-orange solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.28 (d, J=6.6 Hz, 6H), 4.39-4.49 (m, 1H), 7.49 (dd, J=5.8, 0.8 Hz, 1H), 7.73 (d, J=7.8 Hz, 1H), 8.52 (d, J=5.6 Hz, 1H), 8.95 (d, J=0.8 Hz, 1H); ESI-MS m/z [M+H]+ 223.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181249B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4d2321cc5bcd48239ebf73c26eac423d |
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| Source note | uspto-grants-2015_11 |
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