Phenylboronic Acid → HCID 57634242, compound

HRID 2109449Notes

Reaction equation

HRID 2109449 reaction equation
Br[C:2]1[O:6][C:5]([N:7]2[CH2:11][C@:10]3([CH:16]4[CH2:17][CH2:18][N:13]([CH2:14][CH2:15]4)[CH2:12]3)[O:9][C:8]2=[O:19])=[CH:4][CH:3]=1.[C:20]1(B(O)O)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:20]1([C:2]2[O:6][C:5]([N:7]3[CH2:11][C@:10]4([CH:16]5[CH2:17][CH2:18][N:13]([CH2:14][CH2:15]5)[CH2:12]4)[O:9][C:8]3=[O:19])=[CH:4][CH:3]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 57634251HCID 57634251, compound

Product 1

HCID 57634242HCID 57634242, compound

Procedure

The title compound was prepared by a method analogous to that described in Example 12 from (R)-3′-(5-bromofuran-2-yl)spiro[1-azabicyclo[2.2.2]octan-3,5′-oxazolidin]-2′-one and phenylboronic acid. The title compound (49 mg) was obtained as a pale-yellow solid, m/z 325 (MH+).

Workup

  1. customThe title compound was prepared by a method analogous to

Sources & evidence

ORD record
ord-343122751e6a4c70a8116c9bcd3d748b
Source dataset
uspto-grants-2009_04
Patent number
US07514567B2

Reaction notes

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