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1,1'-Carbonyldiimidazole → HCID 86649581, compound

HRID 2066796
Notes
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Reaction equation

HRID 2066796 reaction equation
[CH:1]1[N:5]=[CH:4][N:3]([C:6](N2C=NC=C2)=[O:7])[CH:2]=1.[CH3:13][C:14]1[N:15]=[C:16]([NH2:31])[S:17][C:18]=1[C:19]1[N:20]=[C:21]([C:24]2([C:27]([F:30])([F:29])[F:28])[CH2:26][CH2:25]2)[S:22][CH:23]=1>C(Cl)Cl>[CH3:13][C:14]1[N:15]=[C:16]([NH:31][C:6]([N:3]2[CH:2]=[CH:1][N:5]=[CH:4]2)=[O:7])[S:17][C:18]=1[C:19]1[N:20]=[C:21]([C:24]2([C:27]([F:30])([F:29])[F:28])[CH2:25][CH2:26]2)[S:22][CH:23]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 682631,1'-CarbonyldiimidazoleHCID 58095730HCID 58095730, compound

Product 1

HCID 86649581HCID 86649581, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

CDI (0.13 g) was added to a stirred solution of 4′-methyl-2-(1-trifluoromethyl-cyclopropyl)-[4,5]bithiazolyl-2′-ylamine (Step 10.2) (0.16 g) in CH2Cl2 (5 mL) at rt. The reaction mixture was then stood for 3 h at 25° C. and the title compound isolated by filtration.

Sources & evidence

ORD record
ord-dbc65e0e25174d29bdec4357ce778c8c
Source dataset
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08293753B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes