Azidotrimethylsilane → HCID 86679958, compound

Temperature

60 °C

To a stirred solution of (Z)-tert-butyl 3-oxo-2,3,6,7-tetrahydro-1H-azepine-1-carboxylate (15 g, 71.1 mmol) in acetonitrile (25 mL) was added trimethylsilylazide (28.2 mL, 213 mmol) followed by Amberlite IRA 900F resin (loading: 2-3 mmol/g, 18 g) and the mixture was heated at 60° C. for 4 hr. After standing at room temperature for 16 hr, the resin was filtered off, washed with acetonitrile and the solvent removed under reduced pressure to give a yellow oil. To a solution of this oil (813 mg, 3.2 mmol) in dry Et2O (20 ml) cooled in an ice-salt bath was added a solution of methyl lithium (1.6 M in Et2O, 2.1 mL, 3.36 mmol) dropwise over 10 mins. After stirring for a further 1.5 hr, saturated NaHCO3 (10 mL) was added and the mixture was extracted with EtOAc (2×20 mL). The combined organic layers were dried over MgSO4 and the solvent removed under reduced pressure to afford a green oil (0.8 g, 81% over four steps). 1H NMR (400 MHz, CDCl3) δ 4.00-2.65 (m, 6H), 2.30-1.60 (m, 4H), 1.55-1.20 (m, 12H).

1. filtrationthe resin was filtered off
2. washwashed with acetonitrile
3. customthe solvent removed under reduced pressure
4. customto give a yellow oil
5. extractionthe mixture was extracted with EtOAc (2×20 mL)
6. dry with materialThe combined organic layers were dried over MgSO4
7. customthe solvent removed under reduced pressure
8. customto afford a green oil (0.8 g, 81% over four steps)

ORD record

ord-a2825f2ab6d74e0da6b2b1e41db0af4c

Source dataset

uspto-grants-2013_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08614206B2