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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218512Generated: October 26, 2026

tert-Butyl (3-aminopropyl)carbamate → N-(3-aminopropyl)-N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/2218512

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (3-aminopropyl)carbamateHCID 2735700—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 68407451HCID 68407451—
ProductN-(3-aminopropyl)-N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamideHCID 68407996—

Reaction Steps

According to the procedure in Example 19, (3-amino-propyl)carbamic acid tert-butyl ester was transformed into tert-butyl 3-(N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamido)propylcarbamate, which was reacted with TFA/dichoromethane (3:2), stirred at room temperature for 30 min, concentrated in vacuo, then dissolved in MeOH and treated with 1M HCl/ether. The resulting precipitate was filtered and dried in vacuo to provide N-(3-aminopropyl)-N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamide (220 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410988B2
Source datasetuspto-grants-2008_08
ORD IDord-e79a91114bc941ad9d61b583e6ea1dc6
Source noteuspto-grants-2008_08