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Glutaric anhydride → HCID 22861973, compound

HRID 260257
Notes
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Reaction equation

HRID 260257 reaction equation
[C:1]1(=[O:8])[O:7][C:5](=[O:6])[CH2:4][CH2:3][CH2:2]1.[CH3:9][O:10][C:11](=[O:46])[C@H:12]([CH2:27][C:28]1[CH:35]=[C:33]([I:34])[C:32]([O:36][C:37]2[CH:44]=[C:42]([I:43])[C:41]([OH:45])=[C:39]([I:40])[CH:38]=2)=[C:30]([I:31])[CH:29]=1)[NH:13][C:14](=[O:26])[CH2:15][CH2:16][CH2:17][C:18]([N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)=[O:19]>>[CH3:9][O:10][C:11](=[O:46])[C@H:12]([CH2:27][C:28]1[CH:35]=[C:33]([I:34])[C:32]([O:36][C:37]2[CH:44]=[C:42]([I:43])[C:41]([OH:45])=[C:39]([I:40])[CH:38]=2)=[C:30]([I:31])[CH:29]=1)[NH:13][C:14](=[O:26])[CH2:15][CH2:16][CH2:17][C:18]([N:20]1[CH2:25][CH2:24][N:23]([C:5](=[O:6])[CH2:4][CH2:3][CH2:2][C:1]([OH:7])=[O:8])[CH2:22][CH2:21]1)=[O:19]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 7940Glutaric anhydrideHCID 22861978HCID 22861978, compound

Product 1

HCID 22861973HCID 22861973, compound

Procedure

This material was prepared using the procedure outlined in Intermediate Preparation 1, step 6 except glutaric anhydride was reacted with N-(4-piperazinocarbonylbutyryl)thyroxine methyl ester hydromide from step 4. This compound was purified by column chromatography (SiO2).

Workup

  1. customThis material was prepared
  2. customThis compound was purified by column chromatography (SiO2)

Sources & evidence

ORD record
ord-33853c55ea364fde9b24dff330aaddda
Source dataset
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05527709

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes