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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480348Generated: October 27, 2026

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

https://huagongshe.com/reaction/480348

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 numberUS06649657B2
Source datasetuspto-grants-2003_11
ORD IDord-b8c1828d9e794854b88d61d869d8a311
Source noteuspto-grants-2003_11