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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114488Generated: November 1, 2026

Ammonium Chloride → HCID 178452046, compound

https://huagongshe.com/reaction/2114488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantHCID 59809539HCID 59809539—
SolventDimethylformamideHCID 6228—
ProductHCID 178452046HCID 178452046—

Reaction Conditions

Temperature120 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432257B2
Source datasetuspto-grants-2008_10
ORD IDord-5b4fe00dafc24761b76e6ab63f51cebf
Source noteuspto-grants-2008_10