HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 7-(Morpholin-4-ylmethyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 939967-94-9 | HCID 59231937 | — |
| Product | 7-(Morpholin-4-ylmethyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 59231948 | 20% |
Reaction Steps
To 4-aminopyrrolo[2,1-f][1,2,4]triazine-7-carbaldehyde(235 mg, 1.45 mmol) in 1,2-dichroloethane (5 ml) was added morpholine (0.25 ml, 2.9 mmol) and sodium triacetoxyborohydride (611 mg, 2.9 mmol). The reaction mixture was stirred at rt under N2 for 16 h. The reaction was quenched with saturated aq. sodium bicarbonate and followed by extraction with CH2Cl2. The organic was dried over Na2SO4, concentrated and purified via column chromatography (5:95 v/v CH3OH—CH2Cl2) to afford 66 mg of the title compound (yield 20%). 1H-NMR (DMSO-d6) δ 7.80 (s, 1H), 7.62 (br, 2H), 6.83 (d, J=4 Hz, 1H), 6.52 (d, J=4 Hz, 1H), 3.75 (s, 2H), 3.51(t, J=4 Hz, 4H), 2.37(t, J=4 Hz, 4H); MS [M+H]+=234; LCMS RT=1.00 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143393B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-0622a17c2f0844f291e5f18a5616a60b |
| Source note | uspto-grants-2012_03 |