HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloro-6-piperidinoquinazoline → HCID 178478384, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloro-6-piperidinoquinazoline | HCID 13421799 | — |
| Reactant | HCID 178507266 | HCID 178507266 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178478384 | HCID 178478384 | 61% |
Reaction Steps
To 2,4-Dichloro-6-piperidin-1-yl-quinazoline (100 mg, 0.365 mmol), in ethanol (5 omL) was added 5-Cyclopropyl-2H-pyrazol-3-ylamine (88 mg 0.71 mmol). The additional resulted in the formation of a white precipitate. The partial solution was stirred for 10 hr and (2-Chloro-6-piperidin-1-yl-quinazolin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine was colleted by filtration to give 80 mg (61% yield). HPLC tr=4.90 min (100%), LCMS m/e 369.31 (M+H), 367.28 (M−H) tr=3.41 min, HNMR (500 MHz, dmso): □12.30–12.25 (1H, bs), 10.67 (1H, s), 7.80–7.85 (1H, s), 7.65 91H, d), 7.50 (1H, d), 6.50 (1H, bs), 3.40 (4H, m0, 2.90 (1H, m), 1.70–1.55 (6H, m), 0.95 (2H, m), 0.70 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07262200B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-af407dcdaae64f1eb122732363d8210a |
| Source note | uspto-grants-2007_08 |