Tributyltin azide → HCID 178497603, compound

HRID 557741Notes

Reaction equation

HRID 557741 reaction equation
[N:1]([Sn](CCCC)(CCCC)CCCC)=[N+:2]=[N-:3].[CH3:17][O:18][C:19]([CH:21]1[CH2:26][CH2:25][CH:24]([C:27]#[N:28])[CH2:23][CH2:22]1)=[O:20]>O1CCOCC1>[CH3:17][O:18][C:19]([CH:21]1[CH2:26][CH2:25][CH:24]([C:27]2[NH:3][N:2]=[N:1][N:28]=2)[CH2:23][CH2:22]1)=[O:20]

Participants

4

Conditions

Temperature
145 °C

Procedure

A mixture of azidotributyltin (1.51 mL, 5.48 mmol), and 4-cyano-cyclohexanecarboxylic acid methyl ester (458 mg, 2.74 mmol) in 1,4 dioxane were sealed in a vial and heated in an oil bath at 145° C. for 4 days. The reaction was concentrated, diluted with aqueous sodium bicarbonate (saturated, 200 mL), washed with ethyl acetate (200 mL), acidified to pH 1 with concentrated HCl, and extracted with ethyl acetate (2×200 mL). The organic layer was washed with brine (200 mL), dried over sodium sulfate, concentrated, and tritrated with mixtures of hexanes and ethyl acetate to give 4-(1H-tetrazol-5-yl)-cyclohexanecarboxylic acid methyl ester (304 mg, 52%) as an off white solid. LCMS calcd for C9H14N4O2 (m/e) 210, obsd 211 (M+H).

Workup

  1. customwere sealed in a vial and
  2. concentrationThe reaction was concentrated
  3. additiondiluted with aqueous sodium bicarbonate (saturated, 200 mL)
  4. washwashed with ethyl acetate (200 mL)
  5. extractionextracted with ethyl acetate (2×200 mL)
  6. washThe organic layer was washed with brine (200 mL)
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-1c69bbb504b54660b7ee4d2b562c40e3
Source dataset
uspto-grants-2011_11
Patent number
US08058299B2

Reaction notes

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