HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098655Generated: October 31, 2026
Sodium methanesulfinate → HCID 86643713, compound
https://huagongshe.com/reaction/1098655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | HCID 86643712 | HCID 86643712 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Heptane | HCID 8900 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86643713 | HCID 86643713 | — |
Reaction Steps
A solution of an appropriately protected ethyl (3-amino-8-bromo-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-acetate derivative of Structure 2c (0.238 mmol), cuprous iodide (204 mg, 1.073 mmol, 4.5 eq.) and sodium methanesulfinate (129 mg, 1.073 mmol, 4.5 eq.) in degassed NMP (5 ml) is heated under inert atmosphere at 140° C. overnight. Then, the mixture is diluted with heptane (5 ml) and AcOEt (5 ml) and filtered over a pad of silica gel with AcOEt as eluent. The solvent is removed in vaccuo and the residue dissolved in AcOEt and H2O. The phases are separated and the aq. phase is extracted twice with AcOEt. The combined org. phases are washed with brine and H2O, dried over Na2SO4 and concentrated in vacuuo to yield the corresponding ethyl (3-amino-8-methanesulfonyl-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-acetate derivative of Structure 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143304B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-dc05b7aeaed04f96b3104bb4e41a7072 |
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| Source note | uspto-grants-2012_03 |
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