Hydrochloric Acid → HCID 86746994, compound

HRID 1588441Notes

Reaction equation

HRID 1588441 reaction equation
[F:1][C:2]([F:34])([CH2:31][CH2:32][CH3:33])[CH:3]([OH:30])[CH2:4][CH2:5][CH2:6][C@H:7]1[C@H:11]([O:12][CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][O:14]2)[CH2:10][C@H:9]([OH:19])[C@@H:8]1[CH2:20]/[CH:21]=[CH:22]\[CH2:23][CH2:24][CH2:25][C:26]([O:28][CH3:29])=[O:27].C(N(CC)CC)C.Cl>C(Cl)Cl>[F:34][C:2]([F:1])([CH2:31][CH2:32][CH3:33])[C:3](=[O:30])[CH2:4][CH2:5][CH2:6][C@H:7]1[C@H:11]([O:12][CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][O:14]2)[CH2:10][C:9](=[O:19])[C@@H:8]1[CH2:20]/[CH:21]=[CH:22]\[CH2:23][CH2:24][CH2:25][C:26]([O:28][CH3:29])=[O:27]

Participants

5

Procedure

To the above solution was added a solution of methyl (Z)-7-[(1R)-(2R,3R,5S)-2-{5,5-difluoro-4(RS)-hydroxyoctyl}-5-hydroxy-3-tetra-hydropyranyloxycyclopentyl]hept-5-enoate (18) (0.244 g) in methylene chloride. The resultant mixture was warmed to -25° C. and stirred for 1 hour. Triethylamine (0.60 ml) was added thereto and the reaction mixture was stirred for additional 30 minutes, poured into 1N hydrochloric acid, and then worked up with the conventional procedure. The obtained product was subjected to silicagel column chromatography to give the titled compound (19).

Workup

  1. stirringthe reaction mixture was stirred for additional 30 minutes

Sources & evidence

ORD record
ord-a788e1697dea4288a3258b51ef2740bc
Source dataset
uspto-grants-1993_06
Patent number
US05221799

Reaction notes

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