HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Propanesulfinamide, 2-methyl-N-[(1S)-1,2,3,4-tetrahydro-5-(2,2,2-trifluoroethoxy)-1-naphthalenyl]-, [S(R)]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | HCID 89852658 | HCID 89852658 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Propanesulfinamide, 2-methyl-N-[(1S)-1,2,3,4-tetrahydro-5-(2,2,2-trifluoroethoxy)-1-naphthalenyl]-, [S(R)]- | HCID 89853330 | 43.2% |
Reaction Steps
To a suspension of L-Selectride (3.90 mL, 3.90 mmol) in THF (1 mL) was added Intermediate 13A (0.45 g, 1.3 mmol) in THF (1 mL) at −50° C. The reaction mixture was warmed up to rt until the reduction was complete. To the reaction mixture was added MeOH (2 mL) and brine (2 mL). The resulting reaction mixture was stirred for 5 minutes, filtered, and the filtrate was concentrated in vacuo. The crude product was dissolved in a small amount of DCM and loaded on a 4 g silica gel cartridge eluting from 0 to 100% EtOAc in hexanes over 15 minutes to give Intermediate 13B (196 mg, 0.561 mmol, 43.1% yield). LCMS=2.09 min [M+1]=350 (Method B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199946B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-c76a0d2ebb1149f6a4eba20ff78349e1 |
| Source note | uspto-grants-2015_12 |