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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300559Generated: November 1, 2026

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

https://huagongshe.com/reaction/2300559

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 (from Preparation 5, Step C, 0.118 g, 0.5 mmol) and N,N-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 (from Preparations 3, 0.093 g, 0.55 mmol) was added. The mixture was stirred for 90 minutes. The reaction was cooled to 0° C., NaBH4 (30.3 mg, 0.801 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 numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-d3de600654c747f5ab89f91ea36f9920
Source noteuspto-grants-2002_12