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(R)-3-fluorooctyl methanesulfonate → (R)-5-Heptyloxy-2-[4-(3-fluorooctyloxy)phenyl]pyrimidine

HRID 1197390
Notes
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Reaction equation

HRID 1197390 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[N:11][C:12]([C:15]2[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=2)=[N:13][CH:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].CS(O[CH2:27][CH2:28][C@H:29]([F:35])[CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])(=O)=O>>[CH2:1]([O:8][C:9]1[CH:14]=[N:13][C:12]([C:15]2[CH:16]=[CH:17][C:18]([O:21][CH2:27][CH2:28][C@H:29]([F:35])[CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])=[CH:19][CH:20]=2)=[N:11][CH:10]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 22850588(R)-3-fluorooctyl methanesulfonateHCID 1357088125-Heptyloxy-2-(4-hydroxyphenyl)pyrimidine

Product 1

HCID 53821088(R)-5-Heptyloxy-2-[4-(3-fluorooctyloxy)phenyl]pyrimidineYield 57%

Procedure

The titled compound was synthesized from 5-heptyloxy-2-(4-hydroxyphenyl)pyrimidine and (R)-3-fluorooctyl methanesulfonate.

Sources & evidence

ORD record
ord-d78204b5817843df9e6505ffce1eed52
Source dataset
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05275756

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes