HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 13338425, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Valinol | HCID 640993 | — |
| Reactant | 7-Chloro-1,3,5-trimethyl-1H-pyrazolo[4,3-d]pyrimidine | HCID 13338407 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13338425 | HCID 13338425 | 45.6% |
Reaction Steps
A mixture of 8 g (0.04 mol) of 7-chloro-1,3,5-trimethyl-1H-pyrazolo[4,3-d]pyrimidine (Ex. 3), 4.5 g (0.045 mol) of L-valinol (2-amino-3-methyl-1-butanol) and 8 ml of triethylamine in 50 ml of dimethylformamide is stirred at 50°-55° C. for 50 hours and evaporated in vacuo. The residue is dissolved in methylene dichloride, washed with a saturated solution of sodium bicarbonate, dried over MgSO4, and evaporated in vacuo. The residue is stirred in pet ether to give 4.8 g (45%) of 2-[1,3,5-trimethyl-1H-pyrazolo[4,3-d]-pyrimidine-7-yl]amino-3-methyl-1-butanol, mp 166°-168° C. from acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04469868 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-268dad0f07be42a0bc82a707200e1df9 |
| Source note | uspto-grants-1984_09 |