L-Pyroglutamic Acid → HCID 57699455, 화합물

HRID 1962418노트

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HRID 1962418 반응식
[C:1]([O:5][C:6](=[O:16])[NH:7][C@@H:8]1[CH2:13][CH2:12][C@@H:11]([CH2:14][OH:15])[O:10][CH2:9]1)([CH3:4])([CH3:3])[CH3:2].CCN(C(C)C)C(C)C.N1C(=O)CC[C@H]1C(O)=O>C(Cl)Cl.CS(C)=O>[C:1]([O:5][C:6](=[O:16])[NH:7][C@@H:8]1[CH2:13][CH2:12][C@@H:11]([CH:14]=[O:15])[O:10][CH2:9]1)([CH3:4])([CH3:2])[CH3:3]

참가 물질

6

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온도
0 °C

실험 절차

To a solution of (3R,6S)-(6-hydroxymethyl-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester (37.5 g, 162.13 mmol) in DCM (310 mL) cooled to −10° C. was added DIPEA (84.75 mL, 495.06 mmol). Then a solution of Pyr.SO3 complex (50%, 69.47 g, 218.25 mmol) in DMSO (225 mL) was slowly added. The reaction mixture was stirred for 2 h at 0° C. The reaction mixture was partitioned between water (150 mL) and DCM (220 mL). The two layers were separated and the aq. layer was extracted twice with DCM (2×150 mL). The combined org. layers were dried over Na2SO4, filtered and concentrated to dryness. The residue was co-evaporated 3 times with toluene and purified over a short pad of silica gel (EA-Hept. 2-1) to afford the title aldehyde as a white solid (33.58 g, 90% yield).

후처리

  1. customThe reaction mixture was partitioned between water (150 mL) and DCM (220 mL)
  2. customThe two layers were separated
  3. extractionthe aq. layer was extracted twice with DCM (2×150 mL)
  4. dry with materiallayers were dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated to dryness
  7. custompurified over a short pad of silica gel (EA-Hept. 2-1)

출처 및 근거

ORD 기록
ord-55e2ebee9aa64314988115def3a83a0f
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08415375B2

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