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5-Bromo-6-chloropyridine-3-carboxylic acid → HCID 86702634, compound

HRID 924140
Notes
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Reaction equation

HRID 924140 reaction equation
[Br:1][C:2]1[C:3]([Cl:11])=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=O.[F:12][C:13]([F:23])([F:22])[S:14][C:15]1[N:20]=[CH:19][C:18]([NH2:21])=[CH:17][CH:16]=1>>[Br:1][C:2]1[C:3]([Cl:11])=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([NH:21][C:18]1[CH:19]=[N:20][C:15]([S:14][C:13]([F:23])([F:22])[F:12])=[CH:16][CH:17]=1)=[O:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 2854335-Bromo-6-chloropyridine-3-carboxylic acidHCID 436250226-[(Trifluoromethyl)sulfanyl]pyridin-3-amine

Product 1

HCID 86702634HCID 86702634, compound

Procedure

The title compound was prepared in an analogous fashion to that described in Stage 169.2 using 5-bromo-6-chloronicotinic acid and 6-(trifluoromethylthio)pyridin-3-amine to afford an off-white powder. HPLC (Condition 4) tR=6.43 min, UPLC-MS (Condition 3) tR=1.15 min, m/z=411.9 [M−H]−.

Workup

  1. customto afford an off-white powder

Sources & evidence

ORD record
ord-114abcb110294bfbaaa45691b0441209
Source dataset
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09278981B2

Reaction notes

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