HCID 4215501, compound → HCID 86585194, compound

HRID 1019164Notes

Reaction equation

HRID 1019164 reaction equation
[CH2:1]([C:8]1[N:12]=[C:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:10][N:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19]([O:23][P:24]([C:31]([C:34]1[CH:39]=[CH:38][C:37]([CH2:40]Br)=[CH:36][C:35]=1[Br:42])([F:33])[F:32])(=[O:30])[O:25][C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:22])([CH3:21])[CH3:20]>>[Br:42][C:35]1[CH:36]=[C:37]([CH2:40][CH:1]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:8]2[N:12]=[C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[O:10][N:9]=2)[CH:38]=[CH:39][C:34]=1[C:31]([P:24](=[O:30])([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])[O:23][C:19]([CH3:22])([CH3:20])[CH3:21])([F:32])[F:33]

Participants

3

Reactant 2

HCID 4215501HCID 4215501, compoundHCID 12016041HCID 12016041, compound

Product 1

HCID 86585194HCID 86585194, compound

Procedure

Starting with 3-benzyl-5-phenyl-1,2,4-oxadiazole and di(tert-butyl)[[2-bromo-4-(bromomethyl)phenyl](difluoro)methyl]phosphonate, the title compound was prepared as an oil by using the same procedure described in Step 3 of Example 4.

Sources & evidence

ORD record
ord-6cf86e86fc1547e6ab71814c2f03f79f
Source dataset
uspto-grants-2002_11
Patent number
US06486142B2

Reaction notes

Loading…