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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | tert-Butyl 2-(2-hydroxyethyl)morpholine-4-carboxylate | HCID 44182317 | — |
| Reactant | 1-Phenyl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide | HCID 46833093 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Morpholin-2-ylethyl)-3-phenyl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide | HCID 54756924 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601722B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-925fb8f9c4614bedbce2345bbef1660d |
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| Source note | uspto-grants-2009_10 |
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