Trifluoroacetic acid → HCID 86595987, compound

HRID 1828974Notes

Reaction equation

HRID 1828974 reaction equation
C(OC(=O)[N:7]([CH:10]([CH3:33])[CH2:11][C:12]1[CH:32]=[CH:31][C:15]2[O:16][CH:17]([CH2:19][NH:20][C:21]([O:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[O:22])[O:18][C:14]=2[CH:13]=1)[CH2:8][CH3:9])(C)(C)C.[F:35][C:36]([F:41])([F:40])[C:37]([OH:39])=[O:38]>ClCCl>[F:35][C:36]([F:41])([F:40])[C:37]([OH:39])=[O:38].[CH2:24]([O:23][C:21](=[O:22])[NH:20][CH2:19][CH:17]1[O:16][C:15]2[CH:31]=[CH:32][C:12]([CH2:11][CH:10]([NH:7][CH2:8][CH3:9])[CH3:33])=[CH:13][C:14]=2[O:18]1)[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1

Participants

4

Procedure

To a solution of 1.58 g (3.3 mmol) of 2G in 10 mL of dichloromethane (distilled over CaH2) was added trifluoroacetic acid at room temperature, and the mixture was allowed to stir at room temperature for 30 minutes. The resulting reaction mixture was concentrated under reduced pressure to dryness and purified by silica gel column chromatography to give 1.6 g (3.3 mmol, 98%) of 2H as a colorless gum (M+H, 371).

Workup

  1. customThe resulting reaction mixture
  2. concentrationwas concentrated under reduced pressure to dryness
  3. custompurified by silica gel column chromatography
  4. customto give 1.6 g (3.3 mmol, 98%) of 2H as a colorless gum (M+H, 371)

Sources & evidence

ORD record
ord-1ccf5995e4c542db83e144cf344b1c14
Source dataset
uspto-grants-2006_06
Patent number
US07060847B2

Reaction notes

Loading…