Methanol → HCID 131723529, compound

HRID 2182182Notes

Reaction equation

HRID 2182182 reaction equation
S(O[C@@H:6]1[CH2:10][C@H:9]([CH2:11][O:12][Si:13]([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14])[O:8][C@@H:7]1[N:20]1[CH:27]=[C:26]([F:28])[C:24]([NH2:25])=[N:23][C:21]1=[O:22])(C)(=O)=O.[N-:29]=[N+:30]=[N-:31].[Li+].CO>>[N:29]([C@H:6]1[CH2:10][C@H:9]([CH2:11][O:12][Si:13]([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:14])[CH3:15])[O:8][C@@H:7]1[N:20]1[CH:27]=[C:26]([F:28])[C:24]([NH2:25])=[N:23][C:21]1=[O:22])=[N+:30]=[N-:31]

Participants

4

Reactant 3

HCID 887MethanolHCID 88163Lithium azideHCID 87970440HCID 87970440, compound

Product 1

HCID 131723529HCID 131723529, compoundYield 75%

Conditions

Temperature
100 °C

Procedure

To a solution of 20 (442 mg, 1.01 mmol) in anhydrous dilmethylformamide (12 mL) was added lithium azide moistened with 10% methanol (265 mg, 4.87 mmol). The reaction mixture was stirred at 100° C. during 2.5 h, and then cooled to room temperature, poured onto ice/water (200 mL) and extracted with chloroform (3×100 mL). Combined extracts were washed with a saturated aqueous sodium hydrogen carbonate solution (2×100 mL), with water (5×100 mL) and then dried over sodium sulphate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography [eluent : methanol (4%) in chloroform] to give pure 21 (291 mg, 75% yield) as a white solid: mp 147-148° C.; UV (ethanol): λmax 242 nm (ε 7700), 283 nm (ε 7400), λmin 226 nm (ε 6600), 264 nm (ε 5800); 1H NMR (DMSO-d6): δ 8.05 (d, 1H, H-6, J6-F5=7.0 Hz), 7.9-7.4 (br d, 2H, NH2), 5.7 (br s, 1H, H-1′), 4.37 (d, 1H, H-2′, J2′-3′=5.5 Hz), 4.3 (m, 1H, H-4′), 4. (m, 1H, H-5′), 3.7 (m, 1H,H-5″), 2.0 (m, 1H, H-3′), 1.8 (m, 1H, H-3″), 0.88 (s, 9H, (CH3)3C—Si), 0.05 (s, 6H, (CH3)2Si); MS (matrix GT): FAB>0 m/z 769 (2M+H)+, 385 (M+H)+, 130 (BH2)+; FAB<0 m/z 1151 (3M−H)−, 767 (2M−H)−, 383 (M−H)−, 128 (B)−; [α]D20=+25 (c, 0.95 DMSO).

Workup

  1. temperaturecooled to room temperature
  2. additionpoured onto ice/water (200 mL)
  3. extractionextracted with chloroform (3×100 mL)
  4. washCombined extracts were washed with a saturated aqueous sodium hydrogen carbonate solution (2×100 mL), with water (5×100 mL)
  5. dry with materialdried over sodium sulphate
  6. customevaporated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography [eluent : methanol (4%) in chloroform]

Sources & evidence

ORD record
ord-3d29c29324d64d3887238b8ccfc379c3
Source dataset
uspto-grants-2005_05
Patent number
US06896900B2

Reaction notes

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