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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642541Generated: October 31, 2026

Hydrochloric Acid → 5-Iodo-3-methyl-9H-pyrido[2,3-b]indole-7-carbonitrile

https://huagongshe.com/reaction/1642541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
Reactant5-Amino-3-methyl-9H-pyrido[2,3-b]indole-7-carbonitrileHCID 16124311—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-Iodo-3-methyl-9H-pyrido[2,3-b]indole-7-carbonitrileHCID 16124312822.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 124 (118 mg, 0.53 mmol) was dissolved in HOAc (2 mL) with H2O (1 mL), and the solution stirred at 0° C. Concentrated HCl (120 μL) in H2O (120 mL) was added, and the reaction stirred for 5 min. Sodium nitrite (54 mg, 0.78 mmol) in H2O (120 μL) was added dropwise, and the red solution stirred for 10 min. A solution of iodine (10 mg) and potassium iodide (129 mg, 0.78 mmol) in H2O (300 μL) was added dropwise, and the brown frothy solution stirred for 30 min at 0° C. and then 30 min while warming to r.t. The reaction was diluted with H2O (5 mL) and extracted with CHCl3. Organics were dried (MgSO4) and concentrated in vacuo. Purification by silica gel chromatography gave 108 mg (61%) of the title compound as a faintly yellow solid. MS (ES) [m+H] calc'd for C13H8IN3, 334; found 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119655B2
Source datasetuspto-grants-2012_02
ORD IDord-0c877b46074a4ddca975047b0f2354bb
Source noteuspto-grants-2012_02