تفاعل #49267

ord-59d0630de42b4180826f17821e743067

معادلة التفاعل

CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
di-tert-butyldicarbonate
CNC
dimethylamine
CC(=O)O
acetic acid
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
sodium triacetoxyborohydride
O=Cc1ccc2[nH]ccc2c1
5-formylindole
CN(C)Cc1ccc2c(ccn2C(=O)OC(C)(C)C)c1
5-(dimethylaminomethyl)-1-(tert-butoxycarbonyl)indole
المردود 36.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfollowed by purification by slurry

الإجراء التجريبي

In a similar manner to Step 1 of Reference Example 4, 5-formylindole (5.27 g, 36.3 mmol) was dissolved in acetonitrile (100 mL), and the solution was treated with di-tert-butyldicarbonate (9.17 mL, 39.9 mmol) and DMAP (44.0 mg, 0.360 mmol), then the mixture was treated with 51% aqueous dimethylamine solution (72.0 mL, 724 mmol), acetic acid (41.6 mL, 727 mmol) and sodium triacetoxyborohydride (46.2 g, 218 mmol), followed by purification by slurry using diisopropyl ether to obtain 5-(dimethylaminomethyl)-1-(tert-butoxycarbonyl)indole (3.61 g, yield 36%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745641B2uspto-grants-2010_06