Reaktion #44807

ord-76b3b4e6e7394c3d9cbbbf0b6207f7ac

Reaktionsgleichung

CN(Cc1ccc(Oc2ccc(Br)cc2)cc1)C[C@H]1CCCN1.Cl
(R)—N-[[4-(4-bromophenoxy)phenyl]methyl]-N-methyl-2-pyrrolidinemethanamine hydrochloride salt
COC(=O)c1ccc(C=O)cc1
methyl 4-formylbenzoate
CCN(C(C)C)C(C)C
diisopropylethylamine
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
sodium triacetoxyborohydride
O=C([O-])O.[Na+]
sodium bicarbonate
COC(=O)c1ccc(CN2CCC[C@@H]2CN(C)Cc2ccc(Oc3ccc(Br)cc3)cc2)cc1
methyl 4-[[(R)-2-[[[[4-(4-bromophenoxy)phenyl]methyl]methyl-amino]methyl]-1-pyrrolidinyl]methyl]benzoate
Ausbeute 86.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwere added sequentially
  2. 2
    Extraktionextracted with ethyl acetate (2×)
  3. 3
    SonstigeThe combined organic extracts were dried
  4. 4
    Einengenconcentrated
  5. 5
    SonstigePurification by flash chromatography on silica gel

Vorschrift

A solution of (R)—N-[[4-(4-bromophenoxy)phenyl]methyl]-N-methyl-2-pyrrolidinemethanamine hydrochloride salt (0.87 g, 2 mmol) and methyl 4-formylbenzoate (346 mg, 2.11 mmol) in dichloroethane (20 mL) was stirred as diisopropylethylamine (0.12 mL, 3 mmol) and sodium triacetoxyborohydride (536 mg, 2.53 mmol) were added sequentially. The reaction was stirred at ambient temperature overnight. The reaction was treated with a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate (2×). The combined organic extracts were dried and concentrated. Purification by flash chromatography on silica gel gave 0.9 g of methyl 4-[[(R)-2-[[[[4-(4-bromophenoxy)phenyl]methyl]methyl-amino]methyl]-1-pyrrolidinyl]methyl]benzoate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737145B2uspto-grants-2010_06