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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethyl trichloromethanesulphonateHCID 90027—
ReactantHCID 22615545HCID 22615545—
ReactantHCID 22615719HCID 22615719—
ProductHCID 10321784HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-c4c91f0c1bfe41daa3718b3d41db9fd2
Source noteuspto-grants-2000_11