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1-Butanol → HCID 62735098, compound

HRID 269068
Notes
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Reaction equation

HRID 269068 reaction equation
ClC1C(C[F:9])=CC=CN=1.[CH3:10][O:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][NH2:17])=[CH:14][CH:13]=1.CC[N:22]([CH:26](C)C)C(C)C.[CH2:29](O)[CH2:30][CH2:31][CH3:32]>CN(C1C=CN=CC=1)C>[F:9][C:32]1[C:26]([NH:17][CH2:16][C:15]2[CH:18]=[CH:19][C:12]([O:11][CH3:10])=[CH:13][CH:14]=2)=[N:22][CH:29]=[CH:30][CH:31]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 2631-ButanolHCID 754524-MethoxybenzylamineHCID 81531DiisopropylethylamineHCID 231603702-Chloro-3-(fluoromethyl)pyridine

Product 1

HCID 62735098HCID 62735098, compoundYield 34%

Reagents, catalysts & solvents 1

HCID 14284
4-(Dimethylamino)pyridine
Catalyst

Conditions

Temperature
140 °C

Procedure

A mixture of commercially available 2-chloro-3-fluoromethylpyridine (10.53 g, 80 mmol), 4-methoxybenzylamine (12.5 mL, 96 mmol), DIPEA (16.5 mL, 96 mmol) and DMAP (150 mg) in n-butanol (20 mL) was refluxed (oilbathtemp. 140° C.) for 12 days. Concentrated in vacuum and directly subjected to chromatography. Silica gel column chromatography gave the title compound as a yellow liquid (6.3 g, 34%). MS (ISP) 233.1 [(M+H)+].

Workup

  1. concentrationConcentrated in vacuum

Sources & evidence

ORD record
ord-1170650d9f1f4e2e927fb9bbfdbdb5b3
Source dataset
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07446113B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes