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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79452Generated: October 29, 2026

Ammonium Chloride → 3-iodo-1-((2-methylthiazol-5-yl)methyl)-1H-indazol-4-amine

https://huagongshe.com/reaction/79452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-methyl-1,3-thiazole-5-carboxylateHCID 12808791—
Reactant4-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)-2-methylthiazoleHCID 67261507—
CatalystIronHCID 23925—
SolventWater ethanolHCID 19096565—
Product3-iodo-1-((2-methylthiazol-5-yl)methyl)-1H-indazol-4-amineHCID 67260955—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution 4-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)-2-methylthiazole (prepared according the method of Example 15, Steps A-D, using ethyl 2-methylthiazole-5-carboxylate) in EtOH/H2O (8 mL/2 mL) was added iron (463 mg, 8.30 mmol) and NH4Cl (44.4 mg, 0.830 mmol). The reaction mixture was heated at 85° C. for 3 hours. The reaction mixture was cooled to ambient temperature and concentrated under reduced pressure. EtOAc/Et3N (40 mL/10 mL) was added to the residue. The mixture was heated at 85° C. for 20 minutes, cooled to 45° C., and filtered through Celite. The Celite pad was washed with MeOH (30 mL). The combined filtrate was concentrated under reduced pressure to remove EtOAc and MeOH. The aqueous suspension was extracted with DCM. The combined organic extracts were dried (Na2SO4) and concentrated under reduced pressure to give the product (156 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-b7db519a758049d18cfb3b47d6db67d7
Source noteuspto-grants-2014_09