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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771168Generated: November 3, 2026

Benzyl [(R)-4-(dimethylamino)-4-oxo-1-(phenylthio)butan-2-YL]carbamate → (3R)-3-Amino-N,N-dimethyl-4-(phenylsulfanyl)butanamide

https://huagongshe.com/reaction/1771168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl [(R)-4-(dimethylamino)-4-oxo-1-(phenylthio)butan-2-YL]carbamateHCID 59803608—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
Product(3R)-3-Amino-N,N-dimethyl-4-(phenylsulfanyl)butanamideHCID 5980365862.9%

Reaction Steps

A suspension of (R)-benzyl 4-(dimethylamino)-4-oxo-1-(phenylthio)butan-2-ylcarbamate (INTERMEDIATE 15, 40 g, 0.10 mol) in 40% HBr in acetic acid (100 ml) was stirred at room temperature for 16 hours and the reaction mixture became homogeneous during this time. The mixture was concentrated to dryness, diluted with water (200 ml) and AcOH (200 ml) and washed with diethyl ether (3×50 ml). The aqueous phase was brought to approximately pH 8-9 with solid Na2CO3 and was extracted with CH2Cl2 (5×) The combined organic phases were dried (MgSO4) and concentrated under reduced pressure to give the title product (15 g, 59%) that was used in the preparation of INTERMEDIATE 17 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248140B2
Source datasetuspto-grants-2016_02
ORD IDord-ea67dccad91442f192d1f0ca7d905b23
Source noteuspto-grants-2016_02