HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylene → HCID 14851849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | HCID 14851835 | HCID 14851835 | — |
| Reactant | HCID 14851942 | HCID 14851942 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14851849 | HCID 14851849 | — |
Reaction Steps
This compound was obtained as described in example 17 by coupling of 6-(2-fluorophenyl)-8-iodo-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine with 2-(2-propynyl)-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one. The product was purified by chromatography in the usual fashion and crystallized from ethyl acetate/ethanol. Recrystallization from ethanol gave light yellow crystals with m.p. 170°-173° C. They contained 0.66 molar amounts of water. The synthesis of the required acetylene is described in Example 27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959361 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-1f1eef57658f408d90f2a3625f3f191e |
| Source note | uspto-grants-1990_09 |