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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339894Generated: October 30, 2026

5-(4-Tert-butylphenyl)-2-methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide → 2-(4-Tert-butylphenyl)-3-hydroxy-3-methylbutane-2-sulfonamide

https://huagongshe.com/reaction/339894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Tert-butylphenyl)-2-methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxideHCID 86705333—
ReactantHCID 178431678HCID 178431678—
ReactantHCID 178440750HCID 178440750—
Product2-(4-Tert-butylphenyl)-3-hydroxy-3-methylbutane-2-sulfonamideHCID 68292561—

Reaction Steps

The further conversion to (S)-3-[5-(4-tert-butylphenyl)-5,6,6-trimethyl-4,4-dioxo-5,6-dihydro-4H-4lambda6-[1,4,3]oxathiazin-2-ylamino]-3-(2-fluorophenyl)propan-1-ol was effected via the 5-(4-tert-butylphenyl)-2-methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide intermediate in analogy to the preparation of (S)-3-[5-(3-bromophenyl)-5,6,6-trimethyl-4,4-dioxo-5,6-dihydro-4H-4lambda6-[1,4,3]oxathiazin-2-ylamino]-3-phenylpropan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895547B2
Source datasetuspto-grants-2014_11
ORD IDord-2c9a85e53bd34a77b6d8e457cf9db90a
Source noteuspto-grants-2014_11