HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207716Generated: October 31, 2026
HCID 86699658, compound → HCID 86699660, compound
https://huagongshe.com/reaction/2207716
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86699658 | HCID 86699658 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86699660 | HCID 86699660 | — |
Reaction Steps
As shown in step 8-ii of Scheme 8, N-[2-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-8-yl)allyl]-6-(6-methyl-3-pyridyl)pyrimidin-4-amine (150 mg, 0.4151 mmol) was dissolved in MeOH and the reaction mixture was placed under an atmosphere of H2. After stirring for 2 hours, the mixture was filtered, concentrated under reduced pressure, and purified by medium pressure silica gel chromatography (0-5% MeOH/DCM) to produce N-(2-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-8-yl)propyl)-6-(6-methylpyridin-3-yl)pyrimidin-4-amine (Compound 1029): LCMS=364.39 (M+H); 1H NMR (300 MHz, CDCl3) δ 9.00 (d, J=2.0 Hz, 1H), 8.63 (s, 1H), 8.20 (dd, J=8.1, 2.3 Hz, 1H), 7.81 (d, J=5.0 Hz, 1H), 7.27 (d, J=4.2 Hz, 1H), 6.82 (d, J=5.1 Hz, 1H), 6.71 (s, 1H), 4.43 (dd, J=5.1, 3.0 Hz, 2H), 4.27 (dd, J=5.1, 3.0 Hz, 2H), 3.56 (m, 3H), 2.62 (s, 3H), 1.32 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376448B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-3a56aaafa5094f2d83ab05442f3b52c9 |
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| Source note | uspto-grants-2016_06 |
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