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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818820Generated: October 26, 2026

Triphenylphosphine → 1-(2-Morpholin-2-ylethyl)-3-phenyl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide

https://huagongshe.com/reaction/1818820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactanttert-Butyl 2-(2-hydroxyethyl)morpholine-4-carboxylateHCID 44182317—
Reactant1-Phenyl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxideHCID 46833093—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Morpholin-2-ylethyl)-3-phenyl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxideHCID 5475692480%

Reaction Steps

To a solution of 1-phenyl-1,3-dihydro-2,1,3-benzothiadiazole2,2-dioxide (0.2 g, 0.8 mmol) in THF (10 mL) was added triphenylphosphine (0.26 g, 1 mmol), tert-butyl 2-(2-hydroxyethyl)morpholine-4-carboxylate (0.2 g, 0.9 mmol) and DIAD (0.2 g, 1 mmol) at 0° C. The mixture was allowed to warm to ambient temperature overnight then concentrated and chromatographed on silica gel (0 to 40% EtOAC in hexane). The resulting mostly pure carbamate was dissolved in dichloromethane (10 mL) and treated with HCL (4 mL, 4M in dioxane). The resulting salt was chromatographed on silica (0 to 100% of (7N NH3/MeOH) in dichloromethane) giving the desired product as a clear oil (0.23 g, 80%). HRMS: calcd for C18H21N3O3S+H+, 360.1376; found (ESI, [M+H]+), 360.1377.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601722B2
Source datasetuspto-grants-2009_10
ORD IDord-925fb8f9c4614bedbce2345bbef1660d
Source noteuspto-grants-2009_10