Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078701Generated: October 30, 2026

Iodine → HCID 178497021, compound

https://huagongshe.com/reaction/2078701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 1-acetyl-1H-thieno[3,2-c]pyrazole-5-carboxylateHCID 57637373—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 178497021HCID 17849702189%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 1-acetyl-1H-thieno[3,2-c]pyrazole-5-carboxylic acid methyl ester [1.3 g, 5.79 mmol, Intermediate (25)] in methanol (30 mL) is added sodium methoxide (25 wt % in methanol). The resulting solution mixture is stirred at 60° C. oil bath for 20 minutes. The oil bath is removed and stirred for 5 minutes. To this is added a solution of iodine (1.76 g, 6.93 mmol) in dimethyl formamide (2 mL). The reaction mixture then heated to 60° C. for 1 hour. The solvent is removed in vacuo. The crude is partitioned between ethyl acetate (100 mL) and water (100 mL) and aqueous layer is further extracted with twice ethyl acetate (25 mL). The combined ethyl acetate phases are washed with brine, dried over sodium sulfate and filtered. The solvent is removed in vacuo to give 3-iodo-1H-thieno[3,2-c]pyrazole-5-carboxylic acid methyl ester [1.58 g, 89%, Intermediate (26)] as light yellow solid; 1H NMR [(CD3)2SO)]: δ 13.80 (1H, brs, NH), 7.947 (1H, s), 3.870 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928231B2
Source datasetuspto-grants-2011_04
ORD IDord-b1e0c9b840d64b179ed0fa87a3802753
Source noteuspto-grants-2011_04