4-Methylmorpholine → HCID 178434660, compound

HRID 57258Notes

Reaction equation

HRID 57258 reaction equation
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([CH3:7])[C:3]=1[C:8]1[S:9][C:10]2[CH:16]=[C:15]([S:17](Cl)(=[O:19])=[O:18])[CH:14]=[CH:13][C:11]=2[N:12]=1.[F:21][C:22]([F:26])([F:25])[CH2:23][NH2:24].CN1CCOCC1>CO>[F:21][C:22]([F:26])([F:25])[CH2:23][NH:24][S:17]([C:15]1[CH:14]=[CH:13][C:11]2[N:12]=[C:8]([C:3]3[C:4]([CH3:7])=[N:5][NH:6][C:2]=3[NH2:1])[S:9][C:10]=2[CH:16]=1)(=[O:19])=[O:18]

Participants

5

Reactant 3

HCID 79724-MethylmorpholineHCID 9773Ethanamine, 2,2,2-trifluoro-HCID 178434647HCID 178434647, compound

Product 1

HCID 178434660HCID 178434660, compoundYield 9.4%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

the title compound (11 mg) was prepared from crude 2-(5-amino-3-methyl-1H-pyrazol-4-yl)-benzothiazole-6-sulfonyl chloride (100 mg, 0.30 mmol), 2,2,2-trifluoroethylamine (48 μL, 0.60 mmol) and PS-NMM (0.320 g, 0.60 mmol) in 5 mL of methanol. MS (m/z, ES+): 392.4 (M+1, 100%). Yield=9%.

Sources & evidence

ORD record
ord-cd3bca2176a44f6cbbc18150cb186b45
Source dataset
uspto-grants-2016_09
Patent number
US09434720B2

Reaction notes

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