HCID 22244679, compound → HCID 22244639, compound

HRID 891147Notes

Reaction equation

HRID 891147 reaction equation
[N:1]([CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]2[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:15][C:14]([C:23]([F:26])([F:25])[F:24])=[N:13]2)=[CH:8][CH:7]=1)=[N+]=[N-]>CC#N>[C:17]1([C:16]2[N:12]([C:9]3[CH:10]=[CH:11][C:6]([CH2:5][CH2:4][NH2:1])=[CH:7][CH:8]=3)[N:13]=[C:14]([C:23]([F:25])([F:26])[F:24])[CH:15]=2)[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

3

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 14 from 1-[4-(2-azidoethyl)phenyl]-5-phenyl-3-(trifluoromethyl)-1H-pyrazole (step 2): MS (ESI) m/z 332 [M+H]+, 373 [M+H+CH3CN]+.

Sources & evidence

ORD record
ord-c807b1eeac34413bb4afb9a4253a3b31
Source dataset
uspto-grants-2006_02
Patent number
US07001917B2

Reaction notes

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