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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771202Generated: October 31, 2026

N-Benzyloxycarbonyl-4-[(3R)-3-amino-1-oxo-4-(phenylthio)butyl]morpholine → (R)-3-amino-1-morpholino-4-(phenylthio)butan-1-one

https://huagongshe.com/reaction/1771202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzyloxycarbonyl-4-[(3R)-3-amino-1-oxo-4-(phenylthio)butyl]morpholineHCID 59186685—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
Product(R)-3-amino-1-morpholino-4-(phenylthio)butan-1-oneHCID 59186675—

Reaction Steps

A suspension of (R)-benzyl 4-morpholino-4-oxo-1-(phenylthio)butan-2-ylcarbamate (INTERMEDIATE 71, 25 g, 60 mmol) in 40% HBr in acetic acid (500 ml) was stirred at room temperature for 50 hrs. The reaction mixture became homogeneous during this time. The reaction mixture was concentrated to dryness, diluted with water (400 ml) and 5% aq. HCl (200 ml) and washed with diethyl ether (3×100 ml). The aqueous phase was brought to pH ˜8-9 with solid Na2CO3 and extracted vigorously with CH2Cl2 (5×). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to give the title product (16.9 g, yield: almost quantitative), which was used in the preparation of Intermediate 73 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248140B2
Source datasetuspto-grants-2016_02
ORD IDord-ec9018f0d1d6441bb946c7df80c5b498
Source noteuspto-grants-2016_02