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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408600Generated: October 25, 2026

1-Chloro-N,N-2-trimethylpropenylamine → 4-{[1-(2-Benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carbonyl]-benzofuran-6-ylmethyl-amino}-butyric acid ethyl ester

https://huagongshe.com/reaction/408600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
Reactant4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl esterHCID 70556474—
Reactant1-(2-Benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carboxylic acidHCID 70557369—
SolventDichloromethaneHCID 6344—
Product4-{[1-(2-Benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carbonyl]-benzofuran-6-ylmethyl-amino}-butyric acid ethyl esterHCID 70556724—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 1-chloro-N,N,2-trimethylpropenylamine (2 eq.) in DCM under nitrogen was added 1-(2-benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carboxylic acid, Intermediate 121 (1 eq.). The solution was stirred at 20° C. for 1 h, then added to a solution of 4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl ester, Intermediate 82 (1.2 eq.) in DCM at 0° C. TEA (2 eq.) was then added and the mixture was stirred at 0° C. for 3 h. The crude was diluted with DCM, washed twice with a saturated aqueous solution of NaHCO3, twice with aqueous HCl (0.5N), twice with water, dried over MgSO4, filtered, concentrated under reduced pressure and purified by chromatography on silica gel (elution with heptane/EtOAc 25/75 to 10/90) to afford 4-{[1-(2-benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carbonyl]-benzofuran-6-ylmethyl-amino}-butyric acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-cb53c0c3503e4d12bdb28cf05cf43ffb
Source noteuspto-grants-2014_06