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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118330Generated: October 31, 2026

Diisopropylethylamine → (1R)-2-{[6-({4-[4-(cyclopentylsulfonyl)phenyl]but-3-ynyl}oxy)hexyl]amino}-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanol

https://huagongshe.com/reaction/2118330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(1R)-2-Amino-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-YL)ethanolHCID 56600231—
Reactant1-{4-[(6-Bromohexyl)oxy]but-1-ynyl}-4-(cyclopentylsulfonyl)benzeneHCID 69119722—
SolventDimethylformamideHCID 6228—
Product(1R)-2-{[6-({4-[4-(cyclopentylsulfonyl)phenyl]but-3-ynyl}oxy)hexyl]amino}-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanolHCID 6911980434.3%

Reaction Steps

To a stirred solution of 1-{4-[(6-bromohexyl)oxy]but-1-ynyl}-4-(cyclopentylsulfonyl) benzene (280 mg) in DMF (10 ml) were added (1R)-2-amino-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanol (WO 0266422 A1) (170 mg) and diisopropylethylamine (165 μl). The mixture was heated at 50° for 22 h before being allowed to cool to room temperature. The mixture was dissolved in EtOAC, washed with brine, dried (MgSO4) and evaporated to dryness. The residual oil was purified on a silica bond elut SPE cartridge (10 g), gradient 0% to 30% [MeOH-aqueous ammonia (10:1)] in DCM (Gradmaster™). The appropriate fractions were evaporated to give the title compound (127 mg) LCMS RT=2.87 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442839B2
Source datasetuspto-grants-2008_10
ORD IDord-4614ae717199451fa1ffa593bc1325cd
Source noteuspto-grants-2008_10