HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 86611600, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 69319639 | HCID 69319639 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 86611600 | HCID 86611600 | 190.9% |
Reaction Steps
This compound was prepared according to General Method 6 (EXAMPLE 3) from (3R)-3-benzyl-3,4-dihydro-8-isopropoxy-10-(trifluoromethyl)-2H-[1,4]oxazino[2,3-f]quinoline (25.8 mg, 0.064 mmol) and NaBH4 (300 mg, 7.9 mmol) in 3 mL TFA, to afford 29.6 mg (95%) of (3R)-3-benzyl-3,4-dihydro-8-isopropoxy-4-(2,2,2-trifluoroethyl)-10-(trifluoromethyl)-2H-[1,4]oxazino[2,3-f]quinoline, a yellow solid, after column chromatography (1:9 EtOAc:hexane). 1H NMR (400 MHz, CDCl3) δ 7.51–7.10 (m, 8H), 5.51 (septet, 1H, J=6.2), 4,29 (d, 1H, J=10.5), 3.91 (m, 2H), 3.70–3.50 (m, 2H), 2.90 (dd, 1H, J=6.3, 13.3), 2.80 (dd, 1H, J=9.2, 13.3), 1.39 (d, 6H, J=6.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214690B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-68b40486caff4b0184bf57c3aa44a83b |
| Source note | uspto-grants-2007_05 |