تفاعل #43404

ord-67728f421e3f4195ad806ed49d11f5d7

معادلة التفاعل

O
water
CCN(CC)CC
triethylamine
Cc1ccc(S(=O)(=O)Cl)cc1
para-toluenesulphonyl chloride
O=c1ccc2ncc(Cl)c3c2n1CC3(O)CO
(4R/S)-3-chloro-4-hydroxy-4-(hydroxymethyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one
Cc1ccc(S(=O)(=O)OCC2(O)Cn3c(=O)ccc4ncc(Cl)c2c43)cc1
product
المردود 95.2%
Cc1ccc(S(=O)(=O)OCC2(O)Cn3c(=O)ccc4ncc(Cl)c2c43)cc1
[(4R/S)-(3-Chloro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl)]methyl 4-methylbenzenesulfonate
المردود 95.2%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe phases separated
  2. 2
    غسيلThe organic phase was washed with saturated aqueous sodium bicarbonate solution
  3. 3
    أخرىthen dried
  4. 4
    أخرىevaporated

الإجراء التجريبي

A suspension of (4R/S)-3-chloro-4-hydroxy-4-(hydroxymethyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one (300 mg, 1.2 mmol) in dichloromethane/tetrahydrofuran/N,N-dimethylformamide (10 ml/10 ml/2 ml) was treated with triethylamine (0.25 ml, 1.8 mmol), para-toluenesulphonyl chloride (220 mg, 1.2 mol) and dibutyltin oxide (15 mg, 0.06 mmol). After 3 hours water was added and the phases separated. The organic phase was washed with saturated aqueous sodium bicarbonate solution then dried and evaporated affording the product (465 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07732460B2uspto-grants-2010_06