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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595899Generated: October 30, 2026

Methyl 5-bromothiophene-2-carboxylate → Methyl 5-(3-aminopropyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/1595899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-bromothiophene-2-carboxylateHCID 605713—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
Reactant5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 54075339—
CatalystTriethylamineHCID 8471—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-(3-aminopropyl)thiophene-2-carboxylateHCID 19989043—

Reaction Steps

5-(3-tert-Butoxycarbonylamino-prop-1 ynyl)-thiophene-2-carboxylic acid methyl ester, A mixture of prop-2-ynyl-carbamic acid tert-butyl ester (1.67 g, 0.011 mmol), 5-bromo-thiophene-2-carboxylic acid methyl ester (2.50 g, 0.011 mmol), tetrakistriphenylphosphine(0) palladium (0.622 g, 0.0538 mmol), Cul (0.102 g, 0.538 mmol) and triethylamine (1.57 mL, 0.011 mmol) in 50 mL acetonitrile under nitrogen was heated at reflux for 16 h. The reaction was cooled to room temperature, diluted with 75 mL EtOAc, washed with 5.5% HCl, water and brine, dried over MgSO4, filtered and concentrated in vacuo to an oil. The product was purified via flash chromatography (9:1 to 4:1 hexanes:EtOAc) to afford the title compound as an oil (2.06 g). MS 313 (M+18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288120B1
Source datasetuspto-grants-2001_09
ORD IDord-d6ca6eaf85ec442692e96c0b10ee928c
Source noteuspto-grants-2001_09