HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80768Generated: October 29, 2026
Methanaminium, N-(1-chloroethylidene)-N-methyl-, chloride (1:1) → HCID 86690253, compound
https://huagongshe.com/reaction/80768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanaminium, N-(1-chloroethylidene)-N-methyl-, chloride (1:1) | HCID 94113 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178424775 | HCID 178424775 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86690253 | HCID 86690253 | — |
Reaction Steps
To a solution of 2-(2,6-dimethylphenyl)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-ol (2.38 g, 6.3 mmol) in DCM (50 mL) at 0° C., was added (1-chloro-ethylidene)-dimethylammonium chloride (Vilsmeier reagent) (2.421 g, 18.91 mmol). The reaction was stirred at 0° C. for 5 min, then at r.t. for 30 min. Saturated aqueous NaHCO3 was added to quench the reaction. The mixture was extracted with DCM three times. The combined organic layers was dried over Na2SO4. After filtration and concentration, the resulting residue was purified via silica gel FCC (0-100% EtOAc/heptane) to give 4-chloro-2-(2,6-dimethylphenyl)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine. 1H NMR (400 MHz, CD2Cl2) δ ppm 7.19-7.27 (m, 1 H), 7.11 (d, J=7.6 Hz, 2 H), 5.80 (s, 1 H), 4.16 (s, 2 H), 3.72 (s, 3 H), 3.32 (t, J=5.9 Hz, 2 H), 3.16 (t, J=5.8 Hz, 2 H), 2.88 (dt, J=13.9, 6.9 Hz, 1 H), 2.11 (s, 6 H), 1.23 (d, J=6.8 Hz, 6 H). MS (ESI+) m/z 396.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846656B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0dee09621f5c487889f9d1a30779b0c8 |
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| Source note | uspto-grants-2014_09 |
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