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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990967Generated: October 30, 2026

Ethanol, 1-ethoxy-2,2,2-trifluoro- → HCID 18416128, compound

https://huagongshe.com/reaction/990967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 1-ethoxy-2,2,2-trifluoro-HCID 9897—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 18416152HCID 18416152—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 18416128HCID 1841612856%

Reaction Steps

This compound was prepared according to General Method 7 (EXAMPLE 5) from 2,3-dihydro-7-isopropoxy-9-(trifluoromethyl)-1H-[1,4]thiazino[3,2-g]quinoline (11 mg, 0.034 mmol), trifluoroacetaldehyde ethyl hemiacetal (49 mg, 0.34 mmol) and NaBH3CN (14 mg, 0.22 mmol) in 0.7 mL TFA to afford 7.8 mg (56%) of 2,3-dihydro-7-isopropoxy-1-(2,2,2-trifluoroethyl)-9-(trifluoromethyl)-1H-[1,4]thiazino[3,2-g]quinoline, a yellow oil, after flash chromatography (9:1 hexanes:EtOAc). Data for 2,3-dihydro-7-isopropoxy-1-(2,2,2-trifluoroethyl)-9-(trifluoromethyl)-1H-[1,4]thiazino[3,2-g]quinoline: 1H NMR (400 MHz, CDCl3) δ 7.62 (s, 1H), 7.21 (broad s, 1H), 7.03 (s, 1H), 5.46 (hept, 1H, J=6.1), 3.97 (q, 2H, J=8.8), 3.77-3.83 (m, 2H), 3.08-3.14 (m, 2H), 1.38 (d, 6H, J=6.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462038B1
Source datasetuspto-grants-2002_10
ORD IDord-ae20732dfa964eb0b339e741488b86e5
Source noteuspto-grants-2002_10