반응 #1771988

ord-23477e94e399431c83971c4eabce59dd

반응 방정식

CI
methyliodide
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
lithium hexamethyldisilazide
CC1C[C@@H](C(=O)OC(C)(C)C)N(C(=O)OC(C)(C)C)C1=O
tert-butyl N-tert-butoxycarbonyl-4-methyl-L-pyroglutamate
CC(C)(C)OC(=O)[C@@H]1CC(C)(C)C(=O)N1C(=O)OC(C)(C)C
Boc-PyroGlu(4,4-dimethyl)-OtBu
수율 54.0%
CC(C)(C)OC(=O)[C@@H]1CC(C)(C)C(=O)N1C(=O)OC(C)(C)C
Tert-butyl N-tert-butoxycarbonyl-4,4-dimethyl-L-pyroglutamate
수율 54.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter an additional 3 hours at −78° C.
  2. 2
    기타the cooling bath was removed
  3. 3
    workup.ADDITION50% saturated aqueous ammonium chloride (40 mL) was added
  4. 4
    추출extracted with ether (2×50 mL)
  5. 5
    세척The combined organic layers were washed with water(2×25 mL), saturated sodium bicarbonate (2×25 mL), brine (50 mL)
  6. 6
    건조dried (Na2SO4)
  7. 7
    여과filtered
  8. 8
    농축concentrated

실험 절차

To a solution of tert-butyl N-tert-butoxycarbonyl-4-methyl-L-pyroglutamate (1.2 g, 4.0 mmol) in tetrahydrofuran (20 mL) stirring at −78° C., was added a 1M solution of lithium hexamethyldisilazide in tetrahydrofuran (4.4 mL, 4.4 mmol) dropwise over 5 minutes. After 30 minutes, methyliodide (0.33 mL, 5.2 mmol) was added. After an additional 3 hours at −78° C., the cooling bath was removed and 50% saturated aqueous ammonium chloride (40 mL) was added. The solution was stirred for 20 minutes, then extracted with ether (2×50 mL). The combined organic layers were washed with water(2×25 mL), saturated sodium bicarbonate (2×25 mL), brine (50 mL), dried (Na2SO4), filtered and concentrated to give Boc-PyroGlu(4,4-dimethyl)-OtBu (0.673 g, 54%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE043298E1uspto-grants-2012_04