HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856902Generated: October 30, 2026
2,2,2-Trifluoroethyl trichloromethanesulphonate → HCID 10321784, compound
https://huagongshe.com/reaction/1856902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethyl trichloromethanesulphonate | HCID 90027 | — |
| Reactant | HCID 22615545 | HCID 22615545 | — |
| Reactant | HCID 22615719 | HCID 22615719 | — |
| Product | HCID 10321784 | HCID 10321784 | — |
Reaction Steps
Proceeding as described in Example 28, Step 1 above, but substituting 1-benzyloxycarbonyl-4-tert-butoxycarbonylpiperazine-2-(R)-carboxylic acid with benzyl 1-benzyloxycarbonyl-4-tert-butoxycarbonylpiperazine-2-(RS)-carboxylate [prepared from 1-benzyloxycarbonyl-4-tert-butoxycarbonylpiperazine-2-(RS)-carboxylic acid as described in Ono, N., et al. Bull. Chem. Soc. Jpn., 51, 2401, (1978)] gave benzyl 1-benzyloxycarbonylpiperazine-2-(RS)-carboxylate. This material was first converted to benzyl 1-benzyloxycarbonyl-4-(2,2,2-trifluoroethyl)piperazine-2-(RS)-carboxylate by reacting it with 2,2,2-trifluoroethyl trichloromethanesulfonate as described in Gao, Y., et al. J. Med. Chem., 33, 39, (1990) and then to N-hydroxy-1-[4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine-1-sulfonyl]-4-(2,2,2-trifluoroethyl)piperazine-2-(RS)-carboxamide by following Example 28, Steps 3-5 described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143744 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-c4c91f0c1bfe41daa3718b3d41db9fd2 |
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| Source note | uspto-grants-2000_11 |
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