Trifluoroacetic acid → HCID 89962923, compound

HRID 337716Notes

Reaction equation

HRID 337716 reaction equation
COC1C=C(OC)C=CC=1C[N:6]([C:32]1[S:36][N:35]=[CH:34][N:33]=1)[S:7]([C:10]1[CH:15]=[C:14]([F:16])[C:13]([O:17][C@H:18]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][C@@H:19]2[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:12][C:11]=1[F:31])(=[O:9])=[O:8].C([SiH](CC)CC)C.FC(F)(F)C(O)=O>ClCCl>[F:31][C:11]1[CH:12]=[C:13]([O:17][C@H:18]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][C@@H:19]2[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)[C:14]([F:16])=[CH:15][C:10]=1[S:7]([NH:6][C:32]1[S:36][N:35]=[CH:34][N:33]=1)(=[O:9])=[O:8]

Participants

5

Reactant 3

HCID 6422Trifluoroacetic acidHCID 12052TriethylsilaneHCID 89962292HCID 89962292, compound

Product 1

HCID 89962923HCID 89962923, compoundYield 80%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The reaction and aftertreatment were conducted in the same manner as in Example 1a by using the N-(2,4-dimethoxybenzyl)-2,5-difluoro-4-{[(1S*,2R*)-2-phenylcycloheptyl]oxy}-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide (140 mg, 0.227 mmol) prepared in Example 7a, triethylsilane (0.3 mL), trifluoroacetic acid (3.0 mL) and dichloromethane (3.0 mL), to yield the title compound (84.4 mg, 80%) as a colorless solid.

Workup

  1. customThe reaction and aftertreatment

Sources & evidence

ORD record
ord-3e63867ad0de4e8b9f49c53e16f06438
Source dataset
uspto-grants-2014_11
Patent number
US08889741B2

Reaction notes

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