HCID 68182039, compound → HCID 86669895, compound

HRID 1506398Notes

Reaction equation

HRID 1506398 reaction equation
C1(C2C(C(F)(F)F)=C([C:16]3[O:17][C:18]4[C:28]5[C:23](=[CH:24][C:25]([CH:29]=[O:30])=[CH:26][CH:27]=5)[CH2:22][CH2:21][C:19]=4[N:20]=3)ON=2)C=CC=CC=1.[C:31]1([C:37]2[O:41][N:40]=[C:39](C3OC4C5C(=CC(C=C)=CC=5)CCC=4N=3)[C:38]=2[C:57]([F:60])([F:59])[F:58])[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1>>[C:31]1([C:37]2[O:41][N:40]=[C:39]([C:16]3[O:17][C:18]4[C:28]5[C:23](=[CH:24][C:25]([CH:29]=[O:30])=[CH:26][CH:27]=5)[CH2:22][CH2:21][C:19]=4[N:20]=3)[C:38]=2[C:57]([F:60])([F:59])[F:58])[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1

Participants

3

Reactant 2

HCID 68182039HCID 68182039, compoundHCID 86669893HCID 86669893, compound

Product 1

HCID 86669895HCID 86669895, compound

Procedure

The titled compound was prepared using the experimental protocol described for Preparation 48C employing 2-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-7-vinyl-4,5-dihydronaphtho[2,1-d]oxazole (Preparation 48E). LC/MS M+1=411.1.

Sources & evidence

ORD record
ord-93833f4330fa44f6a5ac57f33b583398
Source dataset
uspto-grants-2015_12
Patent number
US09216972B2

Reaction notes

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