Tetrahydrofuran → HCID 69735894, compound

HRID 497417Notes

Reaction equation

HRID 497417 reaction equation
C(O[C:4](=O)[CH:5]([C:16]1[C:21]([NH:22][C:23]([O:25][CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[O:24])=[CH:20][CH:19]=[C:18]([O:33][CH3:34])[N:17]=1)S(C1C=CC(C)=CC=1)(=O)=O)C.[CH3:36][C:37](C)([O-:39])C.[K+].C1C[O:45][CH2:44]C1>>[CH2:37]([O:39][C:44](=[O:45])[CH:4]=[CH:5][C:16]1[C:21]([NH:22][C:23]([O:25][CH2:26][C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)=[O:24])=[CH:20][CH:19]=[C:18]([O:33][CH3:34])[N:17]=1)[CH3:36]

Participants

4

Reactant 3

HCID 8028Tetrahydrofuran2×HCID 23665647Potassium tert-butoxideHCID 69736562HCID 69736562, compound

Product 1

HCID 69735894HCID 69735894, compound

Procedure

To a cooled (5° C.) solution of 15.7 g (0.031 mol) of (3-benzyloxycarbonylamino-6-methoxy-pyridin-2-yl)-(toluene-4-sulfonyl)-acetic acid ethyl ester dissolved in 160 mL of THF is added, dropwise, 31 mL of a 1N solution of potassium-t-butoxide dissolved in THF. The reaction mixture is warmed to room temperature and stirred for 2 hours. The reaction is quenched with 5 mL of water and evaporated. The residue is dissolved in 200 mL of ethyl acetate and 200 mL of water. The ethyl acetate layers are dried (Na2SO4) and evaporated. The residue is chromatographed on 375 grams of silica gel using 7/3 hexanes/ethyl acetate as the eluant. Appropriate fractions are combined and evaporated to yield 5.57 grams of 3-[3-benzyloxycarbonylamino-6-methoxy-pyridin-2-yl]-acrylic acid ethyl ester. 1H NMR (CDCl3) δ 7.8 (m, 2H), 7.4 (m, 2H), 7.0 (m, 1H), 6.8 (m, 1H), 6.7 (m, 1H), 5.2 (s, 2H), 4.2 (q, 2H), 3.9 (s, 3H), 1.3 (t, 3H). Mass spectrum: m/e=357 (p+1). Step 6:

Workup

  1. additionis added
  2. customThe reaction is quenched with 5 mL of water
  3. customevaporated
  4. dissolutionThe residue is dissolved in 200 mL of ethyl acetate
  5. dry with materialThe ethyl acetate layers are dried (Na2SO4)
  6. customevaporated
  7. customThe residue is chromatographed on 375 grams of silica gel using 7/3 hexanes/ethyl acetate as the eluant
  8. customevaporated

Sources & evidence

ORD record
ord-18f8f6606dcf4b8a826ff2fd25c1d98f
Source dataset
uspto-grants-2005_09
Patent number
US06949562B2

Reaction notes

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