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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783411Generated: October 30, 2026

Triphenylphosphine → 3,3,3-Trifluoro-propane-1-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-(6-methoxy-pyridin-3-ylmethyl)-amide

https://huagongshe.com/reaction/1783411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(6-Methoxypyridin-3-yl)methanolHCID 12259941—
Reactant3,3,3-Trifluoro-propane-1-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-amideHCID 86610741—
SolventTetrahydrofuranHCID 8028—
Product3,3,3-Trifluoro-propane-1-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-(6-methoxy-pyridin-3-ylmethyl)-amideHCID 86610742—

Reaction Steps

3,3,3-Trifluoro-propane-1-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-amide (0.15 g, 0.31 mmol), (6-methoxy-pyridin-3-yl)-methanol (0.06 g, 0.38 mmol), triphenyl phosphine (0.17 g, 0.62 mmol) were dissolved in dry THF (15 ml) at 0-5° C. (ice-water bath) under an argon atmosphere followed by the dropwise addition of diisopropyl azodicarboxylate (0.12 ml, 0.62 mmol) in dry THF (1.5 ml). The reaction mixture was further stirred for 1 h at r.t. and then concentrated under reduced pressure. The crude oil was purified over silica gel (first: heptane-ethylacetate, 97:3-0:100; second: dichloromethane-methanol, 98:2-90:10): white solid 214 mg (81%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501406B2
Source datasetuspto-grants-2009_03
ORD IDord-7e703a008be9493abeef0a61165c3243
Source noteuspto-grants-2009_03