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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | 4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl ester | HCID 70556474 | — |
| Reactant | 1-(2-Benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carboxylic acid | HCID 70557369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-{[1-(2-Benzo[b]thiophen-3-yl-acetyl)-2-methyl-azetidine-2-carbonyl]-benzofuran-6-ylmethyl-amino}-butyric acid ethyl ester | HCID 70556724 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759334B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-cb53c0c3503e4d12bdb28cf05cf43ffb |
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| Source note | uspto-grants-2014_06 |
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