HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5,6-Dihydro-3-hydroxy-2-phenylthiazolo-[2,3-a]isoquinolinium hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromophenylacetyl chloride | HCID 598182 | — |
| Reactant | 1,2,3,4-Tetrahydroisoquinoline-1-thione | HCID 2824212 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5,6-Dihydro-3-hydroxy-2-phenylthiazolo-[2,3-a]isoquinolinium hydroxide | HCID 19020401 | — |
Reaction Steps
(aa) Method A: 23.65 g of 3,4-dihydroisoquinoline-1(2H)-thione was dissolved in 750 ml of chloroform, whereupon the solution was treated at room temperature while cooling firstly with 54 g of α-bromophenylacetyl chloride and 90 minutes later with 53 ml of triethylamine and the mixture was stirred at room temperature overnight. The reaction mixture was washed with water, dried over magnesium sulfate and evaporated in vacuo. There was obtained 5,6-dihydro-3-hydroxy-2-phenylthiazolo[2,3-a]isoquinolinium hydroxide (internal salt) of m.p. 210° (dec.) (from acetonitrile/dioxane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735940 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-93339589deef4af0a2fb35920b737029 |
| Source note | uspto-grants-1988_04 |