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Hydrogen iodide → 4-Iodo-6-(2,3-difluoro-4-methoxyphenyl)pyrimidine

HRID 1751980
Notes
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Reaction equation

HRID 1751980 reaction equation
[F:1][C:2]1[C:7]([F:8])=[C:6]([O:9][CH3:10])[CH:5]=[CH:4][C:3]=1B(O)O.Cl[C:15]1[CH:20]=[C:19](Cl)[N:18]=[CH:17][N:16]=1.[IH:22]>>[I:22][C:15]1[CH:20]=[C:19]([C:3]2[CH:4]=[CH:5][C:6]([O:9][CH3:10])=[C:7]([F:8])[C:2]=2[F:1])[N:18]=[CH:17][N:16]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 24841Hydrogen iodideHCID 709434,6-DichloropyrimidineHCID 250672722,3-Difluoro-4-methoxybenzeneboronic acid

Product 1

HCID 513550004-Iodo-6-(2,3-difluoro-4-methoxyphenyl)pyrimidine

Procedure

The compound was prepared according to Example 1 using 2,3-difluoro-4-methoxyphenylboronic acid and 4,6-dichloropyrimidine. The resultant chloro compound was converted to iodo with hydroiodic acid as described in the general procedure.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-645c0b9f63b24d948f074bc3641f0819
Source dataset
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09162987B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes