HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955802Generated: October 31, 2026
HCID 22141400, compound → HCID 69968568, compound
https://huagongshe.com/reaction/1955802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22141400 | HCID 22141400 | — |
| Reactant | HCID 36689801 | HCID 36689801 | — |
| Reactant | HCID 69967892 | HCID 69967892 | — |
| Product | HCID 69968568 | HCID 69968568 | — |
Reaction Steps
The title compound was prepared by coupling (R)-α-(1,3-benzodioxol-5-yl)benzeneethanamine (preparation described in Step B of Example 60) with (R)-N-[3-[2-iodo-1-[(triethylsilyl)oxy]ethyl]-2-chlorophenyl]methanesulfonamide (prepared from 2-bromo-1-[4-chloro-3-[(methylsulfonyl)amino]phenyl]ethanone, preparation described in Example 69, utilizing the procedures described in step A-C of Example 19) following the procedure described in steps D and E of Example 19 with the following modifications. 1) Chromatography on silica gel using 25% EtOAc/hexane yielded (R), (R)-N-[5-[1-(triethylsilyl)oxy-2-[[1-(1,3-benzodioxol-5-yl)-2-phenylethyl]amino]ethyl]-2-chlorophenyl]methanesulfonamide. 2) In step E the title compound was eluted from silica gel using 1:1 EtOAc/hexane prior to final preparative HPLC purification (see Example 1 for HPLC protocol) eluting with 52% solvent B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05776983 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-4c8a3a9cf5794d25a2e3b61a7aae2c41 |
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| Source note | uspto-grants-1998_07 |
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