HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 178452046, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 59809539 | HCID 59809539 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178452046 | HCID 178452046 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a solution of 4-(3-cyanophenoxazin-10-yl)-piperidine-1-carboxylic acid tert-butyl ester, 4a (0.29 g; 0.68 mmol) in DMF (7 mL) were added sodium azide (0.13 g, 2.0 mmol) and ammonium chloride (0.11 g; 2.06 mmol), and the mixture was heated at 120° C. for 16 h. The mixture was allowed to cool to rt, and filtered. The filtrate was acidified with 1N hydrochloric acid (10 mL) and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried over MgSO4, filtered, and evaporated, yielding 4-[3-(1H-tetrazol-5-yl)-phenoxazin-10-yl]-piperidine-1-carboxylic acid tert-butyl ester, 5a. MS m/z (M+Na) 456.9. The crude material was used as such for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432257B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-5b4fe00dafc24761b76e6ab63f51cebf |
| Source note | uspto-grants-2008_10 |