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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111233Generated: November 1, 2026

Iodine → HCID 178483141, compound

https://huagongshe.com/reaction/2111233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 57637329HCID 57637329—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178483141HCID 17848314151.4%

Reaction Steps

To dimethyl-(1H-thieno[3,2-c]pyrazol-5-ylmethyl)-amine [1 g, 5.51 mmol, Intermediate (5)] in solution in dimethylformamide (10 mL) is added iodine (2.1 g, 8.3 mmol) and potassium hydroxide (0.930 g, 16.5 mmol). The dark solution is stirred at room temperature for 5 hours. Sodium bisulfite (1.5 g) in solution in water is added. The resulting suspension is extracted twice with ethyl acetate. The organic layer is dried over magnesium sulfate and concentrated. The residue is chromatographed through silica gel (ethyl acetate—1.0M ammonia in methanol, 90:10 as eluant) to produce (3-iodo-1H-thieno[3,2-c]pyrazol-5-ylmethyl)-dimethyl-amine [0.87 g, 51%, Intermediate (6)] as a beige powder. LC/MS: RT=1.20 minutes, 307.98 m/e (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07518000B2
Source datasetuspto-grants-2009_04
ORD IDord-376d2a23929d4515a686f0bbbf03f947
Source noteuspto-grants-2009_04