Benzyl azide → HCID 68989761, compound

HRID 1752555Notes

Reaction equation

HRID 1752555 reaction equation
[C:1]([O:5][CH3:6])(=[O:4])[C:2]#[CH:3].C(N([Sn:14]([CH2:23][CH2:24][CH2:25][CH3:26])([CH2:19][CH2:20][CH2:21][CH3:22])[CH2:15][CH2:16][CH2:17][CH3:18])C(=O)OC)C.[CH2:27]([N:34]=[N+:35]=[N-:36])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[CH2:27]([N:34]1[C:2]([C:1]([O:5][CH3:6])=[O:4])=[C:3]([Sn:14]([CH2:15][CH2:16][CH2:17][CH3:18])([CH2:19][CH2:20][CH2:21][CH3:22])[CH2:23][CH2:24][CH2:25][CH3:26])[N:36]=[N:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1

Participants

4

Conditions

Temperature
70 °C

Procedure

Methyl propiolate (5.75 g, 68.4 mmol) was added to methyl ethyl(tributylstannyl)carbamate (26.9 g, 68.6 mmol) in a large sealed tube. The mixture was heated to 70° C. overnight. The mixture was cooled to ambient temperature and the vial was stirred unsealed for 10 minutes. Benzyl azide (10.2 mL, 81.6 mmol) was added, and the vial was resealed and heated to 130° C. overnight. The mixture was purified by silica gel chromatography eluting with a gradient of 5-40% ethyl acetate in hexanes to afford the title compound. MS (ESI+) m/z 508.3 (M+H)+.

Workup

  1. temperatureThe mixture was cooled to ambient temperature
  2. temperatureheated to 130° C. overnight
  3. customThe mixture was purified by silica gel chromatography
  4. washeluting with a gradient of 5-40% ethyl acetate in hexanes

Sources & evidence

ORD record
ord-c8d95635356d44fda29e516bfbd21449
Source dataset
uspto-grants-2015_10
Patent number
US09163007B2

Reaction notes

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