Hydrochloric Acid → HCID 53655601, compound

HRID 726816Notes

Reaction equation

HRID 726816 reaction equation
C[O:2][C:3](=[O:26])[CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[O:12][C:11]2[CH:13]=[C:14]([CH:17]([OH:25])[CH2:18][CH2:19][C:20]3[S:21][CH:22]=[CH:23][CH:24]=3)[CH:15]=[CH:16][C:10]=2[O:9]1.[OH-].[Li+].Cl>O.C1COCC1>[OH:25][CH:17]([C:14]1[CH:15]=[CH:16][C:10]2[O:9][CH:8]([CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:26])=[O:2])[O:12][C:11]=2[CH:13]=1)[CH2:18][CH2:19][C:20]1[S:21][CH:22]=[CH:23][CH:24]=1

Participants

6

Conditions

Temperature
23 °C

Procedure

A mixture of (±)-methyl-5-[[6-(1-hydroxy-3-(2-thienyl)propyl-1,3-benzodioxolyl]pentanoate (Compound 73, 35 mg, 0.093 mmol) and lithium hydroxide (0.37 ml of a 0.5N solution in H2O, 0.186 mmol) in THF (0.74 mL) was stirred at 23° C. for 16 hours. The mixture was acidified with 1N HCl and extracted with EtOAc. The organic portion was dried (MgSO4) filtered and concentrated in vacuo. Flash column chromatography (silica gel, 100% EtOAc) afforded 33.3 mg (99%) of the title compound. 1H NMR (300 MHz, CDCl3) δ 12.0 (brs, 1H), 7.14 (d, J=5.1 Hz, 1H), 7.00 (s, 1H), 6.93 (dd, J=3.3, 5.1 Hz, 1H), 6.83 (d, J=3.3 Hz, 1H), 6.59 (s, 1H), 5.91 (s, 2H), 4.87-4.92 (m, 1H), 2.97 (t, J=5.4 Hz, 2H), 2.43-2.47 (m, 2H), 2.32 (t, J=6.9 Hz, 2H), 1.86-2.18 (m, 2H), 1.44-1.64 (m, 5H).

Workup

  1. extractionextracted with EtOAc
  2. dry with materialThe organic portion was dried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-30fa31112b8440d2bd99cfa559d5c3a9
Source dataset
uspto-grants-1998_01
Patent number
US05710288

Reaction notes

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