4-Methylmorpholine → HCID 178491269, compound

HRID 57253Notes

Reaction equation

HRID 57253 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.[CH3:21][O:22][C:23]1[CH:30]=[CH:29][C:26]([CH2:27][NH2:28])=[CH:25][CH:24]=1.CN1CCOCC1>CO>[CH3:21][O:22][C:23]1[CH:30]=[CH:29][C:26]([CH2:27][NH:28][S:17]([C:15]2[CH:14]=[CH:13][C:11]3[N:12]=[C:8]([C:3]4[C:4]([CH3:7])=[N:5][NH:6][C:2]=4[NH2:1])[S:9][C:10]=3[CH:16]=2)(=[O:19])=[O:18])=[CH:25][CH:24]=1

Participants

5

Reactant 3

HCID 79724-MethylmorpholineHCID 754524-MethoxybenzylamineHCID 178434647HCID 178434647, compound

Product 1

HCID 178491269HCID 178491269, compoundYield 11.6%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

the title compound (15 mg) was prepared from crude 2-(5-amino-3-methyl-1H-pyrazol-4-yl)-benzothiazole-6-sulfonyl chloride (100 mg, 0.30 mmol), 4-methoxybenzylamine (79 μL, 0.60 mmol) and PS-NMM (0.320 g, 0.60 mmol) in 5 mL of methanol. MS (m/z, ES+): 430.5 (M+1, 100%). Yield=11%.

Sources & evidence

ORD record
ord-8b122ac6c0944b438bf71f1368181170
Source dataset
uspto-grants-2016_09
Patent number
US09434720B2

Reaction notes

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