Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 68770255 | HCID 68770255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66786963 | HCID 66786963 | 53.7% |
Reaction Steps
To a cooled (−78° C.) solution of 6-(benzothiazol-2-yloxy)-1H-indole-2-carboxylic acid methyl ester (200 mg, 0.61 mmol) in THF (6 mL) was added LAH (2 M in THF, 0.34 mL, 0.31 g, 0.68 mmol) and the reaction mixture was stirred (−78° C., 1 h). The reaction mixture was treated with H2O (5 mL) and EtOAc (10 mL). The organic layer was separated and the aqueous layer was extracted with EtOAc (2×25 mL). The organic layer was dried, filtered and concentrated in vacuo. The resulting residue was purified by silica gel flash chromatography using MeOH (0.2 M NH3):DCM (0-4%) to provide the title compound as a beige solid (97 mg, 53%). MS (ESI): mass calcd. for C16H12N2O2S, 296.1; m/z found, 297.1 [M+H]+. 1H NMR (400 MHz, CDCl3): 8.63 (s, 1H), 7.72 (d, J=8.1, 1H), 7.64 (dd, J=8.0, 0.7, 1H), 7.57 (d, J=8.5, 1H), 7.41-7.31 (m, 2H), 7.27-7.21 (m, 1H), 7.07 (dd, J=8.5, 2.2, 1H), 6.39 (s, 1H), 4.80 (d, J=5.9, 2H), 1.87 (t, J=5.9, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399465B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-85d3929986234b74aff94c582d05610f |
|---|
| Source note | uspto-grants-2013_03 |
|---|