(5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ⁶,2,6-thiadiazin-3-one

Base Information

• Chemical Name: (5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ⁶,2,6-thiadiazin-3-one
• CAS No.: 537012-78-5
• Molecular Formula: C₁₇H₂₁F₃N₂O₂S
• Molecular Weight: 374.427

Synonyms:(5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ⁶,2,6-thiadiazin-3-one

Chemical Property of (5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ⁶,2,6-thiadiazin-3-one

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Technology Process of (5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ⁶,2,6-thiadiazin-3-one

There total 1 articles about (5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ⁶,2,6-thiadiazin-3-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 78.0%

isopropyl 4,4,4-trifluoro-3-oxobutanoate (175230-50-9) + C13H20N2S → (5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ6,2,6-thiadiazin-3-one (537012-78-5)

Guidance literature:

In toluene; Heating;

Reference yield: 72.0%

(5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ6,2,6-thiadiazin-3-one (537012-78-5) → 1-cyclohexyl-5-trifluoromethyl-2H,3H-1λ4,2,6-thiadiazin-3-one (537012-98-9) + 1-benzyl-1-cyclohexyl-5-trifluoromethyl-3H-1λ6,2,6-thiadiazin-3-one (537012-80-9)

Guidance literature:

With toluene-4-sulfonic acid; In methanol; at 20 ℃;

Reference yield:

(5R,S)-1-benzyl-1-cyclohexyl-5-hydroxy-5-trifluoromethyl-4,5-dihydro-3H-1λ6,2,6-thiadiazin-3-one (537012-78-5) → 3-benzylamino-1-cyclohexyl-5-trifluoromethyl-1λ4,2,6-thiadiazine

Guidance literature:

Multi-step reaction with 3 steps

1: 4-toluenesulfonic acid / methanol / 20 °C

2: 37 percent / CH₂Cl₂ / 20 °C

3: 64 percent / CH₂Cl₂ / Heating

With toluene-4-sulfonic acid; In methanol; dichloromethane;

upstream raw materials:

isopropyl 4,4,4-trifluoro-3-oxobutanoate

Downstream raw materials:

1-cyclohexyl-5-trifluoromethyl-2H,3H-1λ⁴,2,6-thiadiazin-3-one

1-benzyl-1-cyclohexyl-5-trifluoromethyl-3H-1λ⁶,2,6-thiadiazin-3-one

1-cyclohexyl-5-trifluoromethyl-1λ⁴,2,6-thiadiazin-3-yl methanesulfonate

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