Trifluoroacetic acid → HCID 68380244, compound

HRID 573629Notes

Reaction equation

HRID 573629 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([NH2:22])[C:5]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=3)=[C:9]([CH:19]([CH3:21])[CH3:20])[S:8][C:6]=2[N:7]=1.[C:23]1([C:29]2[N:34]=[CH:33][C:32]([S:35](Cl)(=[O:37])=[O:36])=[CH:31][CH:30]=2)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.[C:39]([OH:45])([C:41]([F:44])([F:43])[F:42])=[O:40]>>[F:42][C:41]([F:44])([F:43])[C:39]([OH:45])=[O:40].[CH3:1][C:2]1[N:7]=[C:6]2[S:8][C:9]([CH:19]([CH3:20])[CH3:21])=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=3)[C:5]2=[C:4]([NH:22][S:35]([C:32]2[CH:33]=[N:34][C:29]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[CH:30][CH:31]=2)(=[O:36])=[O:37])[CH:3]=1

Participants

4

Reactant 3

HCID 6422Trifluoroacetic acidHCID 242294636-Phenylpyridine-3-sulfonyl chlorideHCID 68324013HCID 68324013, compound

Product 1

HCID 68380244HCID 68380244, compound

Procedure

Following general method outlined in Example 52, starting from 6-methyl-2-(1-methylethyl)-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-4-amine (40 mg, 0.128 mmol) (Description 21) and 6-phenyl-3-pyridinesulfonyl chloride (39 mg, 0.154 mmol), the title compound (12.2 mg) was isolated as a TFA salt. LCMS (B) m/z: 530 [M+1]+, Rt 3.02 min.

Sources & evidence

ORD record
ord-673b0e8b47294e6e98784032b93157ec
Source dataset
uspto-grants-2015_05
Patent number
US09029545B2

Reaction notes

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