تفاعل #1827407

معادلة التفاعل

2-benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]propanamide

2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]propanamide

sodium hydride

2'-[(t-butoxycarbonylamino)methyl]-1,1'-biphenyl-4-methanol

→

product

المردود 84.0%

2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-benzazepin-3(R)-yl]-propanamide

المردود 84.0%

المذيبات

dimethylformamide

dimethylformamide

ظروف التفاعل

المعالجة

1. 1
   غسيلwas rinsed with 1.0 mL of dimethylformamide which
2. 2
   workup.ADDITIONwas added to the reaction mixture
3. 3
   workup.STIRRINGAfter stirring at 0° C. for 15 minutes
4. 4
   workup.ADDITIONthe reaction mixture was diluted with 400 mL of ethyl acetate and 50% saturated ammonium chloride
5. 5
   أخرىThe mixture was transferred to a separatory funnel
6. 6
   أخرىthe aqueous layer was separated
7. 7
   غسيلThe organic layer was washed with 100 mL of saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride
8. 8
   تجفيفThe organic layer was dried over magnesium sulfate
9. 9
   ترشيحfiltered
10. 10
    أخرىthe solvent removed under vacuum
11. 11
    أخرىThe residue was purified by flash chromatography on silica gel eluting with ethyl acetate/hexane (55:45)

الإجراء التجريبي

To a solution of 819 mg (2.07 mmol) of 2-benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]propanamide (Step A) in 7.0 mL of dry dimethylformamide under nitrogen at 0° C. was added 83 mg (2.1 mmol) of 60% sodium hydride/oil dispersion. After stirring for 15 minutes, a solution of 810 mg (2.1 mmol) of 2'-[(t-butoxycarbonylamino)methyl]-1,1'-biphenyl-4-methanol, methanesulfonate ester (Step F) in 2.0 mL of dimethylformamide was added by cannula. The flask which originally contained the methanesulfonate ester was rinsed with 1.0 mL of dimethylformamide which was added to the reaction mixture. After stirring at 0° C. for 15 minutes, the reaction mixture was diluted with 400 mL of ethyl acetate and 50% saturated ammonium chloride. The mixture was transferred to a separatory funnel and the aqueous layer was separated. The organic layer was washed with 100 mL of saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride. The organic layer was dried over magnesium sulfate, filtered and the solvent removed under vacuum. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate/hexane (55:45) to afford 1.2 g (84%) of the product as a white foam. 1H NMR (200 MHz, CDCl3): δ 1.38 (s, 9H), 1.48 (s, 3H), 1.52 (s, 3H), 1.78 (s, 1H), 2.35-2.70 (m, 3H), 4.18 (d, 6 Hz, 2H), 4.38-4.62 (m, 2H), 4.82 (d, 16 Hz, 1H), 5.05 (s, 2H), 5.25 (d, 16 Hz, 1H), 5.32 (s, 1H), 7.08 (d, 6 Hz, 1H), 7.12-7.43 (m, 18H). FAB-MS: calculated for C41H46N4O6 690; found 691(M+H).

المصدر