تفاعل #71286

معادلة التفاعل

(R)-(1-((2-amino-2,3-dihydro-1H-inden-5-yl)methyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanol

triethylamine

2-chlorobenzenesulfonyl chloride

→

title compound

المردود 31.5%

(R)—N-(5-((4-(hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)methyl)-2,3-dihydro-1H-inden-2-yl)-2-chlorobenzenesulfonamide

المردود 31.5%

المذيبات

tetrahydrofuran

DMSO

ظروف التفاعل

المعالجة

1. 1
   تركيزThe reaction was concentrated to dryness
2. 2
   أخرىto give a brown residue which
3. 3
   أخرىpurified on preparative basic HPLC

الإجراء التجريبي

(R)-(1-((2-amino-2,3-dihydro-1H-inden-5-yl)methyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanol (0.064 mmol, 20 mg) was dissolved in tetrahydrofuran (1 mL) and triethylamine (0.128 mmol, 17.8 μL) followed by 2-chlorobenzenesulfonyl chloride (0.064 mmol, 13.6 mg) and the solution stirred at room temperature overnight. The reaction was concentrated to dryness to give a brown residue which was dissolved in DMSO (1 mL) and purified on preparative basic HPLC to give the title compound (9.8 mg, 0.02 mmol, 31.5%) MS (ESI): m/z [M−H]− 484.4.

المصدر