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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402984Generated: October 31, 2026

Acetic Acid → N-[(2S)-2-(tert-butoxycarbonylamino)-3-(phenylmethoxy)propyl]-N-[2-(tert-butoxycarbonylamino)-3-(phenylmethoxy)Propyl]amine

https://huagongshe.com/reaction/402984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-tert-butyl 3-(benzyloxy)-1-oxopropan-2-ylcarbamateHCID 11196731—
ReactantN2-Boc-(S)-3-(benzyloxy)propane-1,2-diamineHCID 60204732—
SolventEthanolHCID 702—
ProductN-[(2S)-2-(tert-butoxycarbonylamino)-3-(phenylmethoxy)propyl]-N-[2-(tert-butoxycarbonylamino)-3-(phenylmethoxy)Propyl]amineHCID 6663998822.1%

Reaction Steps

The product from Example 17B (0.35 g, 1.25 mmol) and the product from Example 17A (0.36 g, 1.29 mmol) in absolute ethanol (12 mL) were treated with sodium cyanoborohydride (94 mg, 1.50 mmol) and a catalytic amount of acetic acid. The resulting mixture was stirred at ambient temperature overnight. The mixture was partitioned between water (40 mL) and ethyl acetate (3×40 mL). The organic layers were combined, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel (hexanes:ethyl acetate, 1:1) to provide the title compound (0.15 g, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741938B2
Source datasetuspto-grants-2014_06
ORD IDord-c3043b3eb76c45b19f141cbb971558a3
Source noteuspto-grants-2014_06