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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252554Generated: October 31, 2026

Sodium Azide → HCID 59425665, compound

https://huagongshe.com/reaction/252554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantHCID 59425563HCID 59425563—
SolventMethanolHCID 887—
ProductHCID 59425665HCID 5942566580%

Reaction Conditions

Temperature75 °C

Reaction Steps

2-[4-(2-Bromoethoxy)phenyl]-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (258 mg, 0.65 mmol), prepared in example 1BA, step A, is combined with NaN3 (144 mg, 2.2 mmol), and MeOH (3.2 mL). This is heated overnight at 75° C. The reaction mixture is then partitioned between CH2Cl2 and H2O. The organic layer is dried and concentrated. Purification by silica gel chromatography (CH2Cl2) yields 2-[4-(2-azidoethoxy)phenyl]-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (187 mg, 80%), compound 266 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-17b1e737f8224aa08d6c2b8c205e5894
Source noteuspto-grants-2011_01