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Sodium Hydroxide → N-[3-(2-Fluorophenyl)acryloyl]-O4-Methyl-L-Tyrosine

HRID 1746560
Notes
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Reaction equation

HRID 1746560 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=[CH:9][C:10]([NH:12][C@H:13]([C:23]([O:25]C)=[O:24])[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)=[O:11].[OH-].[Na+]>CO>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=[CH:9][C:10]([NH:12][C@H:13]([C:23]([OH:25])=[O:24])[CH2:14][C:15]1[CH:16]=[CH:17][C:18]([O:21][CH3:22])=[CH:19][CH:20]=1)=[O:11]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 86655467HCID 86655467, compound

Product 1

HCID 86655506N-[3-(2-Fluorophenyl)acryloyl]-O4-Methyl-L-TyrosineYield 76%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

The same procedures as in Example 90 were carried out from the compound obtained in Example 38 (5.8 g), 1 mol/L of an aqueous sodium hydroxide solution (24 mL), and methanol (200 mL), to give the captioned compound (4.2 g, 76%) as crystals.

Sources & evidence

ORD record
ord-ad39b11125a7451180d4cb387cb09de9
Source dataset
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09150510B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes