Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | HCID 58380550 | HCID 58380550 | — |
| Product | HCID 52934559 | HCID 52934559 | 56.5% |
Reaction Steps
Using the same reaction conditions and workup as described for the preparation of Example 21A, 1-benzyloxymethyl-cyclopropanesulfonic acid [7-(2-fluoro-4-iodo-phenylamino)-6-methyl-5-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyridin-8-yl]-amide (0.2 g, 0.321 mmol) was reacted with BF3OEt2(0.79 mL, 6.24 mmol) and ethane thiol (0.2 mL, 3.21 mmol). The resulting mixture was stirred at 40° C. for 6 hours. Purification by column chromatography on silica gel (2% MeOH in CHCl3) afforded 100 mg of the product (55% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08466289B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-6aeb10d7fb76484787b9e4cc0233fe3c |
|---|
| Source note | uspto-grants-2013_06 |
|---|