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HCID 178500550, compound → HCID 178520545, compound

HRID 480233
Notes
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Reaction equation

HRID 480233 reaction equation
ClC1C=CC2NC(C3C=CC(N)=CC=3)=NC=2C=1.C[O:19][C:20](=[O:49])[CH:21]([CH2:42][CH:43]1[CH2:48][CH2:47][CH2:46][CH2:45][CH2:44]1)[CH2:22][C:23]([NH:25][C:26]1[CH:31]=[CH:30][C:29]([C:32]2[NH:36][C:35]3[CH:37]=[CH:38][C:39]([Cl:41])=[CH:40][C:34]=3[N:33]=2)=[CH:28][CH:27]=1)=[O:24]>>[Cl:41][C:39]1[CH:38]=[CH:37][C:35]2[NH:36][C:32]([C:29]3[CH:28]=[CH:27][C:26]([NH:25][C:23](=[O:24])[CH2:22][CH:21]([CH2:42][CH:43]4[CH2:48][CH2:47][CH2:46][CH2:45][CH2:44]4)[C:20]([OH:49])=[O:19])=[CH:31][CH:30]=3)=[N:33][C:34]=2[CH:40]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 178500550HCID 178500550, compoundHCID 178507426HCID 178507426, compound

Product 1

HCID 178520545HCID 178520545, compound

Procedure

This compound was prepared by the procedure described in Example 1 part (b) from N-[4-(5-Chloro-1H-benzoimidazol-2-yl)-phenyl]-2-cyclohexylmethyl-succinamic acid methyl ester, and was isolated as an HCl salt.

Workup

  1. customThis compound was prepared by the procedure

Sources & evidence

ORD record
ord-debdce11891b4507aa2bf9190e93250e
Source dataset
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06649642B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes