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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53661Generated: October 26, 2026

Isoamylamine → n[3(s)-Benzyloxycarbonylamino-2(r)-hydroxy-4-phenylbutyl]n-isoamylamine

https://huagongshe.com/reaction/53661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamylamineHCID 7894—
Reactant(2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutaneHCID 9861019—
SolventIsopropanolHCID 3776—
Productn[3(s)-Benzyloxycarbonylamino-2(r)-hydroxy-4-phenylbutyl]n-isoamylamineHCID 1043012481%

Reaction Steps

Part C. A solution of N-benzyloxycarbonyl 3(S)-amino-1,2-(S)-epoxy-4-phenylbutane (30.1 g, 0.10 mol) and 165 mL of isoamylamine in 150 mL of isopropyl alcohol was heated to reflux for 2.5 hours. The solution was cooled to room temperature, concentrated in vacuo and then recrystallized. The product was isolated by filtration and from ethylacetate/hexane to afford 31.7 g (81%) of N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620977
Source datasetuspto-grants-1997_04
ORD IDord-70465559ef8e43ae9e4252e327a48eef
Source noteuspto-grants-1997_04