تفاعل #453012

ord-2199bd41981b475f8f119f432e08d0de

معادلة التفاعل

Oc1cncc(Br)c1
5-bromo-3-hydroxypyridine
c1ccc(P(c2ccccc2)c2ccccc2)cc1
Triphenylphosphine
CCOC(=O)/N=N/C(=O)OCC
DEAD
CC(C)(C)OC(=O)N1CC[C@H]1CO
1-BOC-2-(S)-azetidinemethanol
CC(C)(C)OC(=O)N1CC[C@H]1COc1cncc(Br)c1
title compound
المردود 47.7%
CC(C)(C)OC(=O)N1CC[C@H]1COc1cncc(Br)c1
5-bromo-3-(1-BOC-2-(S)-azetidinylmethoxy)pyridine
المردود 47.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.STIRRINGthe reaction rnixture was stirred for 40 hours at room temperature
  3. 3
    أخرىThe volatiles were removed under vacuum
  4. 4
    أخرىthe residue was triturated with hexane
  5. 5
    أخرىThe hexane was removed
  6. 6
    أخرىthe residue was chromatographed on a silica gel column
  7. 7
    غسيلeluting with hexane:Et2O 10:1 to 10:2

الإجراء التجريبي

Triphenylphosphine (4.01 g, 15.3 mmol) and DEAD (2.43 mL, 15.3 mmol) were dissolved in 30 mL of THF at 0° C., and the mixture was stirred for for 10 minutes. Samples of 1-BOC-2-(S)-azetidinemethanol (2.86 g, 15.3 mmol), prepared as described above, and 5-bromo-3-hydroxypyridine (1.505 g, 10.2 mmol) were added, and the reaction rnixture was stirred for 40 hours at room temperature. The volatiles were removed under vacuum, and the residue was triturated with hexane. The hexane was removed, and the residue was chromatographed on a silica gel column, eluting with hexane:Et2O 10:1 to 10:2 to afford the title compound as a colorless oil (1.669 g). MS (CI/NH3) m/z 344 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.42 (s, 9H), 2.31 (m, 2H), 3.89 (m, 2H), 4.12 (m, 1H), 4.322 (m, 1H), 4.52 (m, 1H), 7.43 (m, 1H), 8.29 (m, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06127386uspto-grants-2000_10