HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 7-[(R)-2-(naphthalen-1-yloxymethyl)pyrrolidin-1-yl]-[1,2,4]-triazolo[1,5-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-Chloro[1,2,4]triazolo[1,5-a]pyrimidine | HCID 21766612 | — |
| Reactant | (R)-2-(naphthalen-1-yloxymethyl)pyrrolidine | HCID 46845432 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 7-[(R)-2-(naphthalen-1-yloxymethyl)pyrrolidin-1-yl]-[1,2,4]-triazolo[1,5-a]pyrimidine | HCID 46842838 | — |
Reaction Steps
400 mg of (R)-2-(naphthalen-1-yloxymethyl)pyrrolidine, 500 mg of the 7-chloro-[1,2,4]triazolo[1,5-a]pyrimidine prepared above and 650 mg of N-ethyldiisopropylamine are heated at 130° C. in a microwave for 3 h in 40 ml of 1-butanol. The butanol is subsequently removed in vacuo, the residue is taken up in ethyl acetate, mixed with water, adjusted to pH 12 using 1 N NaOH solution, phases are separated, the organic phase is dried over sodium sulfate, evaporated and chromatographed on silica gel, giving 640 mg of “A1”; m.p. 74-75°;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546406B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-8a5b501d001b44a7a4ad7671b0cd41dd |
| Source note | uspto-grants-2013_10 |