تفاعل #70407

ord-b89e527a7f1b42b1aa87e72b6cd6ab43

معادلة التفاعل

CC(C)OC(=O)N=NC(=O)OC(C)C
diisopropyl azodicarboxylate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(O)=S
thioacetic acid
C[C@]12CC[C@H]3[C@@H](C[C@H](O)C4C[C@@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2O
androstane-3β,6α,17β-triol
CC(=O)S[C@@H]1CC[C@@]2(C)C(C1)[C@@H](O)C[C@H]1[C@@H]3CC[C@H](O)[C@@]3(C)CC[C@@H]12
3α-acetylthioandrostane-6α,17β-diol
المردود 66.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter 2 hrs at 0° C.
  2. 2
    غسيلThe mixture was washed with water
  3. 3
    أخرىthe organic layer evaporated to dryness
  4. 4
    أخرىThe crude product was purified by flash chromatography (SiO2, cyclohexane:EtOAc 55:45)

الإجراء التجريبي

To a solution of triphenylphosphine (2.38 g) in THF (140 mL) cooled at 0° C., diisopropyl azodicarboxylate (1.79 mL) was added dropwise. After stirring for 30 minutes, thioacetic acid (0.65 mL) and androstane-3β,6α,17β-triol (2.00 g) were added. After 2 hrs at 0° C. and overnight at room temperature EtOAc was added. The mixture was washed with water and the organic layer evaporated to dryness. The crude product was purified by flash chromatography (SiO2, cyclohexane:EtOAc 55:45) to give 3α-acetylthioandrostane-6α,17β-diol (1.60 g, 66%). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 4.42 (1H, bb), 4.28 (1H, bb), 3.91 (1H, bb), 3.42 (1H, m), 3.11 (1H, m), 2.28 (3H, s), 2.00-0.80 (20H, m), 0.74 (3H, s), 0.60 (3H, s).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08536160B2uspto-grants-2013_09