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3,4-Dichloropyridine → HCID 19072374, compound

HRID 1073555
Notes
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Reaction equation

HRID 1073555 reaction equation
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]([NH2:11])[CH:3]=1.[Cl:12][C:13]1[CH:14]=[N:15][CH:16]=[CH:17][C:18]=1Cl>C(O)(C)C>[ClH:12].[Cl:12][C:13]1[CH:14]=[N:15][CH:16]=[CH:17][C:18]=1[NH:11][N:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:2]([CH3:1])=[CH:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 27360813,4-DichloropyridineHCID 124272923-Methyl-1H-indol-1-amine

Product 1

HCID 19072374HCID 19072374, compound

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

The title compound was prepared from 3-methyl-1H-indol-1-amine and 3,4-dichloropyridine in isopropanol at 80° C. for 5 hours in substantially the same manner as in Example 1. Recrystallized from ethanol, m.p. 278°-280° C. (decomp.).

Workup

  1. customRecrystallized from ethanol, m.p. 278°-280° C. (decomp.)

Sources & evidence

ORD record
ord-388d280de03042c9b0aa95827d9472f3
Source dataset
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04970218

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes