Cyclopentane-1,3-diol → HCID 11669947, compound

HRID 2381576Notes

Reaction equation

HRID 2381576 reaction equation
Cl[C:2]1([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[N:3]1[CH2:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=1.[CH:27]1([OH:33])[CH2:31][CH2:30][CH:29]([OH:32])[CH2:28]1>>[Cl:19][C:16]1[CH:17]=[CH:18][C:13]([CH2:12][N:3]2[C:2]([C:20]3[CH:21]=[CH:22][C:23]([Cl:26])=[CH:24][CH:25]=3)([O:32][CH:29]3[CH2:30][CH2:31][CH:27]([OH:33])[CH2:28]3)[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[C:4]2=[O:11])=[CH:14][CH:15]=1

Participants

3

Reactant 2

HCID 100165Cyclopentane-1,3-diolHCID 51351392HCID 51351392, compound

Product 1

HCID 11669947HCID 11669947, compound

Procedure

3-Chloro-2-(4-chlorobenzyl)-3-(4-chlorophenyl) isoindolin-1-one (157 mg, 0.390 mmol) was reacted with 1,3-cyclopentanediol (0.18 mL, 1.95 mmol.) as for general procedure C and the solvent evaporated under vacuum to leave a clear oil of crude 2-(4-chlorobenzyl)-3-(4-chlorophenyl)-3-(3-hydroxycyclopentyloxy)isoindolin-1-one. This was purified by HPLC to give the pure product which was a clear glass (83 mg, 0.177 mmol., 45%). Rf 0.08 (40:60 EtOAc:petrol). λmax (CH3OH)/nm=220.5 (Abs=1.333). IR: 3426, 2935, 1696, 1695, 1597, 1489, 1467 cm−1. 1H NMR (300 Hz, DMSO); δ1.03-1.86 (m, 6H, cyclopentanediol C—H), 2.02 (m, 1H, N—CH2), 3.48-3.75 (M, 1H, N—CH2), 4.00-4.50 (m, 2H, cyclopentanediol O—C—H), 6.66-7.15 (m, 9H, Ar—H), 7.32-7.53 (m, 2H, Ar—H), 7.83 (m, 1H, Ar—H). 13C NMR (75 Hz, DMSO); δ 31.4 (N—CH2), 32.1, 33.8, 34.0, 42.9, 44.1 (cyclopentanediol), 95.0 (Ar2C(O)—N), 72.1, 73.0 (cyclopentanediol C—OH), 124.0, 124.3, 128.5, 128.6, 130.2, 130.8, 130.8, 132.7 (Ar). LC/MS-ES+ m/z 470.3, 468.3, 245.1, 243.1. Anal. Calcd. for C26H23Cl2NO3.0.4H2O: C, 65.66; H, 5.04; N, 2.95%. Found C, 65.49; H, 4.94; N, 3.02%. HRMS (EI) m/z: 467.1055. Found 467.1055.

Workup

  1. customthe solvent evaporated under vacuum

Sources & evidence

ORD record
ord-1ea3e920a2274f44ac43397adb4aa128
Source dataset
uspto-grants-2012_09
Patent number
US08258175B2

Reaction notes

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