Imidazole → HCID 22270368, compound

HRID 1987261Notes

Reaction equation

HRID 1987261 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH:9]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[CH:14]=2)[CH:10](O)[CH3:11])=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[NH:39]1C=CN=C1.CCOC(/[N:49]=[N:50]/C(OCC)=O)=O>C(Cl)Cl>[N:39]([CH:10]([CH:9]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[CH:14]=1)[CH2:8][C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=1)[CH3:11])=[N+:49]=[N-:50]

Participants

6

Reactant 4

HCID 795ImidazoleHCID 11776TriphenylphosphineHCID 5462977Diethyl azodicarboxylateHCID 222704984-(4-Chlorophenyl)-3-(3-fluorophenyl)-2-butanol

Product 1

HCID 22270368HCID 22270368, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a mixture of 4-(4-chlorophenyl)-2-(3-fluorophenyl)-2-butanol (Step C, 0.65 g, 2.3 mmol), triphenylphosphine (1.2 g, 4.7 mmol), imidazole (0.32 g, 4.7 mmol) and zinc azide dipyridine complex (Viaud, M. C.; Rollin, P. Synthesis 1990, 130) (0.72 g, 2.3 mmol) in 10 mL CH2Cl2 was added diethylazodicarboxylate (0.73 mL, 4.7 mmol) at 0° C. After stirring at room temperature for 30 min, the resulting mixture was concentrated with silica gel (20 g) and loaded onto a silica gel column, which was eluted with 2% ether in hexane to 2% ammonia in MeOH (2 M) in 2% ether/hexane to give the title compound. 1H NMR (400 MHz, CD3OD): δ 7.25-6.85 (m, 8H), 3.76 (m, 1H), 3.33 (m, 1H), 2.92 (m, 2H), 1.15 (d, 3H).

Workup

  1. concentrationthe resulting mixture was concentrated with silica gel (20 g)
  2. washwas eluted with 2% ether in hexane to 2% ammonia in MeOH (2 M) in 2% ether/hexane

Sources & evidence

ORD record
ord-1f0419a6a89c41a3bc440eb96d699d6c
Source dataset
uspto-grants-2009_06
Patent number
US07550489B2

Reaction notes

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