L-Pyroglutamic Acid → HCID 57699455、化合物

HRID 1962418ノート

反応式

HRID 1962418 の反応式
[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]

参加物

6

反応条件

温度
0 °C

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-55e2ebee9aa64314988115def3a83a0f
出典データセット
uspto-grants-2013_04
特許番号
US08415375B2

反応ノート

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