Hexane → HCID 57704765, compound

HRID 607099Notes

Reaction equation

HRID 607099 reaction equation
[F:1][C:2]([F:51])([F:50])[C:3]1[CH:4]=[C:5]([C@H:13]2[O:17][C:16](=[O:18])[N:15]([CH2:19][C:20]3[CH:25]=[C:24]([C:26]([F:29])([F:28])[F:27])[CH:23]=[C:22]([I:30])[C:21]=3[C:31]3[CH:32]=[C:33]([C:38]4[CH:43]=[CH:42][C:41]([C:44]([O:46]C)=[O:45])=[CH:40][C:39]=4[CH3:48])[CH:34]=[CH:35][C:36]=3[Cl:37])[C@H:14]2[CH3:49])[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.O[Li].O.CCOC(C)=O.CCCCCC>O1CCOCC1>[F:51][C:2]([F:1])([F:50])[C:3]1[CH:4]=[C:5]([C@H:13]2[O:17][C:16](=[O:18])[N:15]([CH2:19][C:20]3[CH:25]=[C:24]([C:26]([F:27])([F:28])[F:29])[CH:23]=[C:22]([I:30])[C:21]=3[C:31]3[CH:32]=[C:33]([C:38]4[CH:43]=[CH:42][C:41]([C:44]([OH:46])=[O:45])=[CH:40][C:39]=4[CH3:48])[CH:34]=[CH:35][C:36]=3[Cl:37])[C@H:14]2[CH3:49])[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1

Participants

6

Procedure

To a solution of the title compound from Step B (30 mg, 0.035 mmol) in dioxane (2 ml) at room temperature, an aqueous solution of LiOH.H2O (7.36 mg, 0.175 mmol) was added. The mixture was stirred at room temperature for overnight. TLC (EtOAc:hexane/2:8) showed no starting material. The solvent was removed. 1N HCl (1 ml) was added. The mixture was extracted with methylene chloride (3×10 ml). The combined methylene chloride layers were dried over sodium sulfate. The title compound was obtained by preparative reverse phase HPLC as a colorless solid.

Workup

  1. customThe solvent was removed
  2. addition1N HCl (1 ml) was added
  3. extractionThe mixture was extracted with methylene chloride (3×10 ml)
  4. dry with materialThe combined methylene chloride layers were dried over sodium sulfate

Sources & evidence

ORD record
ord-0e418a389ab2464fb8cce97d4eb79833
Source dataset
uspto-grants-2011_03
Patent number
US07915271B2

Reaction notes

Loading…