HCID 66726836, compound → HCID 25174838, compound

HRID 2365955Notes

Reaction equation

HRID 2365955 reaction equation
[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:3][C@@H:2]1[C:11]([N:13]1[CH2:18][CH2:17][CH2:16][C@@H:15]([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:28])([F:27])[F:26])[CH:20]=2)[CH2:14]1)=O>C1COCC1>[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:3][C@@H:2]1[CH2:11][N:13]1[CH2:18][CH2:17][CH2:16][C@@H:15]([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:27])([F:26])[F:28])[CH:20]=2)[CH2:14]1

Participants

3

Reactant 1

HCID 66726836HCID 66726836, compound

Product 1

HCID 25174838HCID 25174838, compoundYield 53.7%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

(R)-2,3-Dihydrobenzo[1,4]dioxin-2-yl-[(S*)-3-(3-trifluoromethylphenyl)piperidin-1-yl]methanone (29 mg, 0.074 mmol) was treated with BH3 THF according to the above general procedure. Flash chromatography gave 15 mg of the title compound.

Sources & evidence

ORD record
ord-98708ecfda88478891b2085036c4d5f2
Source dataset
uspto-grants-2014_04
Patent number
US08697723B2

Reaction notes

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