تفاعل #1095878

ord-b2d5f4c1d3c242f19daff95fd826babf

معادلة التفاعل

[Cl-].[NH4+]
ammonium chloride
C[C@@H]1C[C@H](C)CN(c2ncnc(Cl)c2F)C1
4-chloro-6-(cis-3,5-dimethylpiperidino)-5-fluoropyrimidine
[H-].[Na+]
sodium hydride
CC#CCO
2-butyn-1-ol
CC#CCOc1ncnc(N2C[C@H](C)C[C@H](C)C2)c1F
4-(2-butynyloxy)-5-fluoro-6-(cis-3,5-dimethylpiperidino)pyrimidine
المردود 90.7%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for 6 hours at 60° C
  2. 2
    استخلاصthe mixture was extracted with tert-butyl methyl ether three times
  3. 3
    غسيلThe organic layers were washed with a saturated sodium chloride aqueous solution
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    تركيزconcentrated

الإجراء التجريبي

0.10 g of sodium hydride (60% oil suspension) was suspended in 3 ml of tetrahydrofuran. 1 ml of tetrahydrofuran solution of 0.16 g of 2-butyn-1-ol was added dropwise therein, and the mixture was stirred for 10 minutes. Into the mixture was added dropwise 1 ml of tetrahydrofuran solution of 0.31 g of 4-chloro-6-(cis-3,5-dimethylpiperidino)-5-fluoropyrimidine and stirred for 6 hours at 60° C. Into the reaction mixture was added a saturated ammonium chloride aqueous solution, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.32 g of 4-(2-butynyloxy)-5-fluoro-6-(cis-3,5-dimethylpiperidino)pyrimidine (hereinafter, referred to as Compound (29)).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07973028B2uspto-grants-2011_07