تفاعل #155353

ord-1a82367606764c0d8c31ebcf550338c2

معادلة التفاعل

CCOC(C)=O.Cl
hydrogen chloride ethylacetate
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(COC(=O)CNCC(=O)OC(C)(C)C)c12
5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-ylmethyl (tert-butoxycarbonylmethylamino)acetate
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(COC(=O)CNC)c12.Cl
5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-ylmethyl methylaminoacetate hydrochloride
المردود 88.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe deposited insoluble matter was collected by filtration
  2. 2
    غسيلwashed with acetone
  3. 3
    أخرىdried

الإجراء التجريبي

A 4N hydrogen chloride ethylacetate solution (1 ml) was added to an ethyl acetate solution (2 ml) of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-ylmethyl (tert-butoxycarbonylmethylamino)acetate (100 mg, 0.19 mmol) and stirred at room temperature for 3 hours. The deposited insoluble matter was collected by filtration, washed with acetone, and then dried, giving a white powder of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-ylmethyl methylaminoacetate hydrochloride (78.3 mg, yield: 88%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE045108E1uspto-grants-2014_09