반응 #1447116

ord-af64c2b412ac4bee8a27543fa9470758

반응 방정식

C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O
2′-C-methylcytidine
C[C](C)(C)[Mg][Cl]
tert-butylmagnesium chloride
CCCCCCCC/C=C\CCCCCCCCOC(=O)[C@H](C)NP(=O)(Cl)Oc1ccc(Cl)cc1
(9Z)-octadec-9-en-1-yl N-[chloro(4-chlorophenoxy)phosphoryl]-L-alaninate
CCCCCCCC/C=C\CCCCCCCCOC(=O)[C@H](C)NP(=O)(OC[C@H]1O[C@@H](n2ccc(N)nc2=O)[C@](C)(O)[C@@H]1O)Oc1ccc(Cl)cc1
title compound
CCCCCCCC/C=C\CCCCCCCCOC(=O)[C@H](C)NP(=O)(OC[C@H]1O[C@@H](n2ccc(N)nc2=O)[C@](C)(O)[C@@H]1O)Oc1ccc(Cl)cc1
5′-O-[(4-chlorophenoxy)[[(1S)-1-methyl-2-[(9Z)-9-octadecenyloxy]-2-oxoethyl]amino]phosphinyl]-2′-C-methylcytidine

용매

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The crude mixture was purified by column chromatography on silica gel (DCM:MeOH gradient from 90:10 to 80:20)
  2. 2
    workup.DISSOLUTIONthe resulting solid was redissolved in DMSO
  3. 3
    기타purified by RP-HPLC

실험 절차

Following the procedure described for Example 1, step 3, 2′-C-methylcytidine in THF (0.097 M) was cooled to −78° C., then tert-butylmagnesium chloride (as 1.0 M solution in THF, 2.2 eq.) was added followed by the addition of (9Z)-octadec-9-en-1-yl N-[chloro(4-chlorophenoxy)phosphoryl]-L-alaninate. The crude mixture was purified by column chromatography on silica gel (DCM:MeOH gradient from 90:10 to 80:20), the resulting solid was redissolved in DMSO and purified by RP-HPLC to afford the title compound as white powders. A 1:1.4* mixture of diastereoisomers at phosphorus was observed by 1H NMR.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07879815B2uspto-grants-2011_02