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Hydrochloric Acid → HCID 66764225, compound

HRID 1453638
Notes
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Reaction equation

HRID 1453638 reaction equation
[Cl:1][C:2]1[N:7]=[N:6][C:5]([C:8]23[CH2:15][N:12]([CH2:13][CH2:14]2)[CH2:11][CH2:10][CH2:9]3)=[CH:4][CH:3]=1.CS[C:18]1[S:22][C:21](B(O)O)=[CH:20][CH:19]=1.Cl.[CH3:27]C(O)C>>[ClH:1].[CH3:27][C:18]1[S:22][C:21]([C:2]2[N:7]=[N:6][C:5]([C:8]34[CH2:15][N:12]([CH2:13][CH2:14]3)[CH2:11][CH2:10][CH2:9]4)=[CH:4][CH:3]=2)=[CH:20][CH:19]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 313Hydrochloric AcidHCID 3776IsopropanolHCID 27946275-(Methylsulfanyl)-2-thienylboronic acidHCID 57528563HCID 57528563, compound

Product 1

HCID 66764225HCID 66764225, compound

Procedure

This compound is obtained according to the method described in stage 1.6 of Example 1, using 5-(6-chloropyridazin-3-yl)-1-azabicyclo[3.2.1]octane, prepared according to stage 1.5 of Example 1, and 5-methylsulfanyl-2-thienylboronic acid. The hydrochloride thereof is prepared by treatment of the base with a solution of hydrochloric acid in propan-2-ol, and the crystals obtained are collected by filtration and dried under vacuum.

Workup

  1. customThis compound is obtained
  2. customprepared
  3. customthe crystals obtained
  4. filtrationare collected by filtration
  5. customdried under vacuum

Sources & evidence

ORD record
ord-9636db97e6c7489e9258909f9499bafc
Source dataset
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07476674B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes