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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699074Generated: October 30, 2026

Diisopropylethylamine → 5-(3-(3-(3-Chloro-phenyl)-propylamino)-propyl)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1699074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3-Chlorophenyl)propionaldehydeHCID 10419579—
ReactantMethyl 5-(3-aminopropyl)thiophene-2-carboxylateHCID 19989043—
SolventMethanolHCID 887—
Product5-(3-(3-(3-Chloro-phenyl)-propylamino)-propyl)-thiophene-2-carboxylic acid methyl esterHCID 5390012097.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-(3-amino-propyl)-thiophene-2-carboxylic acid methyl ester (0.118 g, 0.5 mmol) and diisopropylethylamine (0.071 g, 0.55 mmol) in 10 mL MeOH was stirred at room temperature for 30 minutes and 3-(3-chloro-phenyl)-propionaldehyde (0.093 g, 0.55 mmol) was added. The mixture was stirred for 90 minutes. The reaction was cooled to 0° C., NaBH4 (0.83 mL, 5.98 mmol) was added and the mixture was stirred for 30 minutes. The reaction was quenched with 1:1 NaHCO3:H2O and was washed with CH2Cl2. The CH2Cl2 extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to afford the title compound as an oil (171 mg). MS 352 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344485B1
Source datasetuspto-grants-2002_02
ORD IDord-3b3487e69c574308ab53f8212f13122b
Source noteuspto-grants-2002_02