HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158482Generated: October 30, 2026
Triphenylphosphine → ((3S*,4R*)-1-benzyl-4-{[isopropyl-(2-nitro-benzenesulfonyl)-amino]-methyl}-pyrrolidin-3-ylmethyl)-isopropyl-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1158482
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | N-isopropyl-2-nitrobenzenesulfonamide | HCID 4154456 | — |
| Reactant | ((3S*,4R*)-1-Benzyl-4-hydroxymethyl-pyrrolidin-3-ylmethyl)-isopropyl-carbamic acid tert-butyl ester | HCID 68616191 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | ((3S*,4R*)-1-benzyl-4-{[isopropyl-(2-nitro-benzenesulfonyl)-amino]-methyl}-pyrrolidin-3-ylmethyl)-isopropyl-carbamic acid tert-butyl ester | HCID 68616510 | — |
Reaction Steps
To a solution of ((3S*,4R*)-1-benzyl-4-hydroxymethyl-pyrrolidin-3-ylmethyl)-isopropyl-carbamic acid tert-butyl ester (0.60 g, 1.66 mmol), N-isopropyl-2-nitro-benzenesulfonamide (0.49 g, 1.99 mmol), and PPh3 (0.52 g, 1.99 mmol) in toluene (15 mL), is added dropwise diisopropyl azodicarboxylate (0.39 mL, 1.99 mmol) at 0° C. under a nitrogen atmosphere. The solution is stirred for 1 h at room temperature, and then heated at 65° C. for 1 h. The reaction mixture is concentrated. The crude material is used purified by flash chromatography on silica gel (eluent: c-hexane/AcOEt 3:7) to give the crude product. To the solid product is added a mixture of Et2O/hexane (1:1) and the resulting suspension is filtered. The solid is washed with Et2O/hexane (1:1) solution, and then the combined filtrate is concentrated to give a titled product. TLC, Rf (AcOEt)=0.61. MS (LC-MS): 589.3 [M+H]+; tR (HPLC, C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/2.5 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 mL/min): 6.39 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807709B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-a806a800d7a247298cb94078a1627a46 |
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| Source note | uspto-grants-2010_10 |
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