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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820149Generated: October 26, 2026

2-Thiophenecarboxaldehyde, 5-chloro- → {4-[(5-Chloro-thiophen-2-ylmethyl)-amino]-2,6-dimethyl-phenyl}-carbamic acid propyl ester

https://huagongshe.com/reaction/1820149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarboxaldehyde, 5-chloro-HCID 81700—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantSodium chloride dihydrateHCID 23713072—
Reactant(4-Amino-2,6-dimethyl-phenyl)-carbamic acid propyl esterHCID 68707091—
SolventMethanolHCID 887—
Product{4-[(5-Chloro-thiophen-2-ylmethyl)-amino]-2,6-dimethyl-phenyl}-carbamic acid propyl esterHCID 1150861949%

Reaction Conditions

Temperature130 °C

Reaction Steps

(4-Amino-2,6-dimethyl-phenyl)-carbamic acid propyl ester (84 mg) and 5-chloro-thiophene-2-carbaldehyde (48 uL) were dissolved in methanol (3 mL) and heated to 130° C. for 5 minutes in a sealed microwave process vial. Sodium cyanoborohydride (95 mg) was added and the reaction mixture was heated to 130° C. for 5 minutes in a sealed microwave process vial, followed by addition of water/brine (1:1, 3 mL). The product was extracted with ethyl acetate (3×3 mL) and the combined organic phases were washed with brine (5 mL), dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography to furnish 66 mg (49% yield) of the title compound as an oil. LC-MS (m/z) 353 (MH+); tR=3.06, (UV, ELSD) 87%, 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601870B2
Source datasetuspto-grants-2009_10
ORD IDord-efce2a94360740d0bc3b9cacfd4823b4
Source noteuspto-grants-2009_10