Methylamine → HCID 86594335, compound

HRID 252037Notes

Reaction equation

HRID 252037 reaction equation
[CH2:1]1[O:13][C:4]2([CH2:10][CH:9]3[C:11](=O)[CH:6]([CH2:7]C3)C2)[O:3][CH2:2]1.CC[N:16]([CH2:19][CH3:20])[CH2:17]C.CN.[BH4-].[Na+]>C1COCC1.CO.Cl[Ti](Cl)(Cl)Cl>[CH2:2]1[O:3][C:4]2([CH:10]3[CH2:9][CH2:11][CH:6]2[CH2:7][CH:19]([NH:16][CH3:17])[CH2:20]3)[O:13][CH2:1]1

Participants

8

Procedure

To a solution of bicyclo[3,2,1]octane-3,8-dione8-ethylene ketal (53.1 mg, 0.27 mmol, 1.0 eq.) in THF (1.0 mL) at 0° C. was added Et3N (0.11 mL, 2.9 eq.) followed by MeNH2 (2.0 M in THF, 0.21 mL, 1.5 eq.). After stirring at room temperature for 5 minutes, TiCl4 (0.30 mL, 10.0 eq.) was introduced dropwise and the resulting mixture was stirred at 0° C. for 45 minutes. A solution of NaBH4 (53.1 mg, 5.1 eq.) in MeOH (2.0 mL) was then introduced and the resulting mixture was stirred at 0° C. for 1 h. The reaction was quenched with saturated NaHCO3 and the separated aqueous layer was extracted with 3×EtOAc. The combined organic phase was dried over MgSO4, filtered and concentrated to give the crude product, 3-methylamino-bicyclo[3,2,1]octan-8-one ethylene ketal (24.1 mg).

Workup

  1. stirringthe resulting mixture was stirred at 0° C. for 45 minutes
  2. stirringthe resulting mixture was stirred at 0° C. for 1 h
  3. customThe reaction was quenched with saturated NaHCO3
  4. extractionthe separated aqueous layer was extracted with 3×EtOAc
  5. dry with materialThe combined organic phase was dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-d36a6458e75b481f8b98433668302c57
Source dataset
uspto-grants-2011_01
Patent number
US07868002B2

Reaction notes

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