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Hydrochloric Acid → N-[(5-isoquinolyl)sulfonyl]-1,3-xylylenediamine

HRID 10603
Notes
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Reaction equation

HRID 10603 reaction equation
C(OC([NH:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([CH2:16][NH:17][S:18]([C:21]2[CH:30]=[CH:29][CH:28]=[C:27]3[C:22]=2[CH:23]=[CH:24][N:25]=[CH:26]3)(=[O:20])=[O:19])[CH:11]=1)=O)(C)(C)C.Cl>CO>[CH:26]1[C:27]2[C:22](=[C:21]([S:18]([NH:17][CH2:16][C:12]3[CH:13]=[CH:14][CH:15]=[C:10]([CH2:9][NH2:8])[CH:11]=3)(=[O:19])=[O:20])[CH:30]=[CH:29][CH:28]=2)[CH:23]=[CH:24][N:25]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 69525002N-(tert-butoxycarbonyl)-N'-[(5-isoquinolyl)sulfonyl]-1,3-xylylenediamine

Product 1

HCID 69524243N-[(5-isoquinolyl)sulfonyl]-1,3-xylylenediamineYield 81%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

According to Reference Example 5, Step C, a reaction was performed by using Intermediate 63 (5 g) and 10% hydrogen chloride in methanol (20 ml) to obtain the title compound (3.1 g).

On this pageParticipantsProcedureSources & evidenceReaction notes

Sources & evidence

ORD record
ord-45adba3b20e14f428e038d8658406cee
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07094789B2

Reaction notes

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