HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azido(trimethyl)stannane → HCID 178441963, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | HCID 9983626 | HCID 9983626 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178441963 | HCID 178441963 | 17% |
Reaction Steps
The title compound was prepared from 3-n-butyl-5-(4-chlorobenzylsulfonyl)-4-[(2'-cyanobiphenyl- 4-yl)methyl]-4H-1,2,4-triazole (Step A) according to the procedure of Example 15, Step E, except that 3.5 equivalents of trimethyltin azide were added at the start, and the column was eluted with a gradient of 0-10% methanol in CH2Cl2. The product was obtained in 17% yield as a glass, which was transformed to a powder upon scraping: mp 180°-182° C. dec.; homogeneous by TLC in 4:1CH2Cl2 --MeOH; mass spectrum (FAB) m/e 548 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05336778 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-cc0d989d23cb4a97952fdf8851d505b8 |
| Source note | uspto-grants-1994_08 |