HCID 58216626, compound → HCID 59525908, compound

HRID 386022Notes

Reaction equation

HRID 386022 reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:17]([OH:20])([CH3:19])[CH3:18])=[CH:12][C:11]=2[F:21])=[CH:5][C:6]=1[C:7]([NH2:9])=[O:8].Cl[C:23]1[N:28]=[C:27]([CH2:29][OH:30])[C:26]([C:31]([OH:34])([CH3:33])[CH3:32])=[CH:25][CH:24]=1>>[F:16][C:15]1[CH:14]=[C:13]([C:17]([OH:20])([CH3:18])[CH3:19])[CH:12]=[C:11]([F:21])[C:10]=1[C:4]1[S:3][C:2]([NH:1][C:23]2[CH:24]=[CH:25][C:26]([C:31]([OH:34])([CH3:33])[CH3:32])=[C:27]([CH2:29][OH:30])[N:28]=2)=[C:6]([C:7]([NH2:9])=[O:8])[CH:5]=1

Participants

3

Procedure

The title compound was prepared as described in Example 1 using 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (105 mg, 0.34 mmol) and 2-[6-chloro-2-(hydroxymethyl)pyridin-3-yl]propan-2-ol (71 mg, 0.35 mmol) as starting materials.

Sources & evidence

ORD record
ord-5a85ed4984834813a4862d6566c22fab
Source dataset
uspto-grants-2013_02
Patent number
US08367706B2

Reaction notes

Loading…