Benzil → HCID 11698084, compound

HRID 2116903Notes

Reaction equation

HRID 2116903 reaction equation
[F:1][C:2]([F:19])([F:18])[C:3]1[C:4]([N:9]2[CH2:14][CH2:13][N:12]([C:15]([NH2:17])=[NH:16])[CH2:11][CH2:10]2)=[N:5][CH:6]=[CH:7][CH:8]=1.[C:20]1([C:26]([C:28]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=O)=O)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:20]1([C:26]2[N:16]=[C:15]([N:12]3[CH2:13][CH2:14][N:9]([C:4]4[C:3]([C:2]([F:1])([F:18])[F:19])=[CH:8][CH:7]=[CH:6][N:5]=4)[CH2:10][CH2:11]3)[NH:17][C:28]=2[C:30]2[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

Participants

3

Procedure

4-(3-(Trifluoromethyl)pyridin-2-yl)piperazine-1-carboxamidine (300 mg, 1.10 mmol, Example 3(a)) reacted with benzil (231 mg, 1.10 mmol, Aldrich) under the conditions of Example 4(b). The crude product was purified by silica gel column chromatography (1:3 EtOAc/hexane) to give the title compound as a white amorphous solid. MS (ESI, pos. ion) m/z: 450.

Workup

  1. customThe crude product was purified by silica gel column chromatography (1:3 EtOAc/hexane)

Sources & evidence

ORD record
ord-7f3e260b5593404eb4883198124cb5d9
Source dataset
uspto-grants-2008_10
Patent number
US07439360B2

Reaction notes

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