HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351957Generated: November 3, 2026
(R)-N-[2-benzyloxy-5-(2-iodo-1-triethylsilyloxyethyl)phenyl]methanesulfonamide → HCID 69456203, compound
https://huagongshe.com/reaction/1351957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (R)-N-[2-benzyloxy-5-(2-iodo-1-triethylsilyloxyethyl)phenyl]methanesulfonamide | HCID 54211801 | — |
| Reactant | HCID 69458689 | HCID 69458689 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69456203 | HCID 69456203 | 37% |
Reaction Steps
To a solution of (R)-3-(2-aminopropyl)-1H-indole-6-carboxylic acid diethylamide (20.0 mg, 0.0742 mmol) in acetonitrile (1.0 ml) is added (R)—N-[2-benzyloxy-5-(2-iodo-1-triethylsilyloxyethyl)phenyl]-methanesulfonamide (41.1 mg, 0.0742 mmol), and the mixture is stirred at 110° C. for 21 hours in a sealed vessel. The reaction solution is concentrated under reduced pressure, and the residue is purified by preparative TLC (a saturated ammonia solution in chloroform/methanol=50/1) to give 3-{(2R)-2-[2-(4-benzyloxy-3-methanesulfonylamino-phenyl)-(2R)-2-(triethylsilyloxy) ethylamino]propyl}-1H-indole-6-carboxylic acid diethylamide (19.2 mg, 0.0272 mmol, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217724B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-841068460b044beabb0dbd934bff8288 |
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| Source note | uspto-grants-2007_05 |
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