HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-(Methylamino)-2-(methylthio)pyrimidin-5-yl)methanol → 4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-(Methylamino)-2-(methylthio)pyrimidin-5-yl)methanol | HCID 10679092 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde | HCID 10607520 | 92% |
Reaction Steps
A mixture of (4-(methylamino)-2-(methylthio)pyrimidin-5-yl)methanol (22.0 g, 119 mmol) and MnO2 (44 g, 714 mmol) in CHCl3 (300 mL) was stirred at RT for 3 h. The reaction was filtered and the filtrate concentrated to give 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carbaldehyde as a pale solid (20 g, 92% yield). 1H NMR (400 MHz, DMSO-d6): δ 9.71 (s, 1H), 8.60 (brs, 1H), 8.49 (s, 1H), 2.96 (d, J=4.8 Hz, 3H), 2.48 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163756B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-ea514eccca424e9f90bc5f9e3db8806c |
| Source note | uspto-grants-2012_04 |