HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-[(1R)-2-({6-[4-(1,1-Dioxido-3,4-dihydro-2H-thiochromen-7-yl)butoxy]hexyl}amino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol formate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | (1R)-1-(2,2-Dimethyl4H-1,3-benzodioxin-6-yl)-2-({6-[4-(1,1-dioxido-3,4-dihydro-2H-thiochromen-7-yl)butoxy]hexyl}amino)ethanol | HCID 69442949 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(1R)-2-({6-[4-(1,1-Dioxido-3,4-dihydro-2H-thiochromen-7-yl)butoxy]hexyl}amino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol formate | HCID 87837188 | — |
Reaction Steps
A solution of (1R)-1-(2,2-dimethyl4H-1,3-benzodioxin-6-yl)-2-({6-[4(1,1-dioxido-3,4-dihydro-2H-thiochromen-7-yl)butoxy]hexyl}amino)ethanol (134 mg) in glacial acetic acid (10 ml) and water (5 ml) was heated at 80° C. for 40 min. The mixture was concentrated in vacuo and the residue purified by mass directed autoprep to give the title compound (79 mg). LCMS RT=2.46 min, ES+ve 520 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07294650B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-ac820dfdf19f4b8a9693d8ab7158ee72 |
| Source note | uspto-grants-2007_11 |