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p-Toluenesulfonic acid monohydrate → HCID 178516181, compound

HRID 1846492
Notes
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Reaction equation

HRID 1846492 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[NH:10][C:11]([CH:13]1[CH2:17][CH2:16][O:15][CH2:14]1)=O.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[Cl:9][C:4]1[C:3]2[NH:10][C:11]([CH:13]3[CH2:17][CH2:16][O:15][CH2:14]3)=[N:1][C:2]=2[CH:7]=[C:6]([OH:8])[CH:5]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 66978176N-(2-amino-6-chloro-4-hydroxyphenyl)tetrahydrofuran-3-carboxamide

Product 1

HCID 178516181HCID 178516181, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

0.10 g (0.39 mmol) N-(2-amino-6-chloro-4-hydroxyphenyl)tetrahydrofuran-3-carboxamide were placed in 20 mL methanol, a spatula tip of p-toluenesulphonic acid monohydrate was added and the mixture was boiled for 2 h. The reaction mixture was evaporated down i.vac. and purified by chromatography. The fractions containing product were combined and evaporated down i.vac.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customThe reaction mixture was evaporated down i.vac
  2. customand purified by chromatography
  3. additionThe fractions containing product
  4. customevaporated down i.vac

Sources & evidence

ORD record
ord-d47bc832bb53472b83595fbb6a198255
Source dataset
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08952014B2

Reaction notes

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