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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942784Generated: October 26, 2026

Acetic Acid → N-((5-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)furan-2-yl)methyl)-2-methoxyethanamine

https://huagongshe.com/reaction/1942784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-MethoxyethylamineHCID 8018—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)furan-2-carbaldehydeHCID 86635185—
SolventDichloromethaneHCID 6344—
ProductN-((5-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)furan-2-yl)methyl)-2-methoxyethanamineHCID 67491421—

Reaction Steps

A suspension of 107 (2.00 g, 5.20 mmol), 2-methoxyethylamine (1.954 g, 26.02 mmol), NaBH(OAc)3 (5.52 g, 26.02 mmol) and acetic acid (1.49 ml, 26.02 mmol) in anhydrous dichloromethane was stirred at room temperature under nitrogen for five days. The reaction mixture was then carefully quenched with a saturated solution of NaHCO3 (pH 8-9), and extracted with DCM. The extract was dried over anhydrous magnesium sulfate, filtered, and concentrated to afford the title compound 108 as a yellow-orange sticky oil. The material was used in the next step without further purification. MS (m/z): 444.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389541B2
Source datasetuspto-grants-2013_03
ORD IDord-82efbb6641e9423e8d2a54a6b0ee8360
Source noteuspto-grants-2013_03