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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158377Generated: November 2, 2026

Ethylamine → HCID 68616941, compound

https://huagongshe.com/reaction/1158377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(3S*,4R*)-3-formyl-4-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 59512275—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 68616941HCID 68616941—

Reaction Steps

The corresponding enantiomer N-((3S,4R)-4-Ethylaminomethyl-pyrrolidin-3-ylmethyl)-N-isopropyl-4-methoxy-3-(3-methoxy-propoxy)-benzamide is obtained as follows: A solution of (3S,4R)-3-formyl-4-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (1.27 g, 2.58 mmol) and gaseous ethylamine (0.704 g, 15.5 mmol; Fluka 02940) in 1,2-dichloroethane (10 mL) is stirred at room temperature for 30 min, then sodium triacetoxyborohydride (1.37 g, 6.45 mmol) is added in one portion and the mixture is stirred overnight. The organic phase is washed with saturated aqueous NaHCO3 solution, the water layers are re-extracted with CH2Cl2, and the combined organics are dried (Na2SO4) and evaporated to dryness to give the title compound. MS: 522.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-cc6ba09f03264f14a8caea61855b0449
Source noteuspto-grants-2010_10