HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(4-Tert-butylphenyl)-2-methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide | HCID 86705333 | — |
| Reactant | HCID 178431678 | HCID 178431678 | — |
| Reactant | HCID 178440750 | HCID 178440750 | — |
| Product | 2-(4-Tert-butylphenyl)-3-hydroxy-3-methylbutane-2-sulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895547B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-2c9a85e53bd34a77b6d8e457cf9db90a |
| Source note | uspto-grants-2014_11 |