HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 7-Methylthieno[3,2-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Chloro-7-methylthieno(3,2-d)pyrimidine | HCID 2777586 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 7-Methylthieno[3,2-d]pyrimidin-4-amine | HCID 57516888 | 78.2% |
Reaction Steps
In a sealed tube was added 4-chloro-7-methylthieno[3,2-d]pyrimidine (2.0 g, 10.83 mmol) and ammonium hydroxide (12.65 mmol, 325 mmol) in butanol (7 ml). The reaction was heated to 90 C for 4 hours and then cooled to room temperature. The resulting white precipitate was collected to give 7-methylthieno[3,2-d]pyrimidin-4-amine (1.4 g, 78% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.41 (1H, s), 7.74 (1H, s), 7.34 (2H, s), 2.34 (3H, d, J=1.00 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278320B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-eef143e26a0e449baefd402e4e31e56e |
| Source note | uspto-grants-2012_10 |