HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

FV-100 free base → HCID 56962118, compound

HRID 1775756
Notes
Print preview

Reaction equation

HRID 1775756 reaction equation
[NH2:1][C@@H:2]([CH:34]([CH3:36])[CH3:35])[C:3]([O:5][CH2:6][C@@H:7]1[C@@H:11]([OH:12])[CH2:10][C@H:9]([N:13]2[CH:18]=[C:17]3[CH:19]=[C:20]([C:22]4[CH:27]=[CH:26][C:25]([CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:24][CH:23]=4)[O:21][C:16]3=[N:15][C:14]2=[O:33])[O:8]1)=[O:4].[ClH:37].CC(O)C>>[ClH:37].[NH2:1][CH:2]([CH:34]([CH3:35])[CH3:36])[C:3]([O:5][CH2:6][C@@H:7]1[C@@H:11]([OH:12])[CH2:10][C@H:9]([N:13]2[CH:18]=[C:17]3[CH:19]=[C:20]([C:22]4[CH:23]=[CH:24][C:25]([CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:26][CH:27]=4)[O:21][C:16]3=[N:15][C:14]2=[O:33])[O:8]1)=[O:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 16063377FV-100 free baseHCID 21912024Isopropanol hydrochloride

Product 1

HCID 56962118HCID 56962118, compound

Procedure

The above reaction mixture from Example 15 was cooled below 5° C. and was added with 20% of HCl IPA solution until pH 1˜4. The mixture was stirred for additional 1 h and was filtered. The filter cake was washed with 34.6 kg of dichloromethane. Desired crude product was obtained. The overall yield from Example 12 was 67% and the purity was 97%. The crude product was recrystallized with methanol/dichloromethane/MTBE to give the desired pure product.

Workup

  1. temperaturewas cooled below 5° C.
  2. filtrationwas filtered
  3. washThe filter cake was washed with 34.6 kg of dichloromethane
  4. custom
Desired crude product was obtained
  • customThe overall yield from Example 12
  • customThe crude product was recrystallized with methanol/dichloromethane/MTBE
  • customto give the desired pure product
  • Sources & evidence

    ORD record
    ord-34dff15e634d459f9e63aedea7ff38c8
    Source dataset
    uspto-grants-2016_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09260469B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes