HCID 67157985, compound → HCID 67157391, compound

HRID 30194Notes

Reaction equation

HRID 30194 reaction equation
Br[C:2]1[O:6][C:5]([CH2:7][CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][N:9]2[C:14]([C:16]2[N:17]=[C:18]([CH3:28])[S:19][C:20]=2[C:21]2[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=2)=[O:15])=[N:4][C:3]=1[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.[Cu][C:36]#[N:37]>>[F:27][C:24]1[CH:25]=[CH:26][C:21]([C:20]2[S:19][C:18]([CH3:28])=[N:17][C:16]=2[C:14]([N:9]2[CH2:10][CH2:11][CH2:12][CH2:13][CH:8]2[CH2:7][C:5]2[O:6][C:2]([C:36]#[N:37])=[C:3]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[N:4]=2)=[O:15])=[CH:22][CH:23]=1

Participants

3

Procedure

The title compound (50 mg) was prepared by treating the compound of example 167 (0.410 g) with copper(I)cyanide (0.103 g) according to the method of example 96. Following column chromatography, further purification by HPLC was required (Supercosil ABZ+, 5-95% acetonitrile containing 0.1% trifluoroacetic acid-water containing 0.1% trifluoroacetic acid).

Workup

  1. customcolumn chromatography, further purification by HPLC

Sources & evidence

ORD record
ord-f7ebaa1b413047099e0c64062fb383d4
Source dataset
uspto-grants-2008_09
Patent number
US07423052B2

Reaction notes

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