Diphenylmethyl acetate → HCID 54381562, compound

HRID 442871Notes

Reaction equation

HRID 442871 reaction equation
C(O[CH:5]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=O)C.[N:18]1([S:24]([C:27]2[NH:28][C:29]3[C:34]([CH:35]=2)=[CH:33][CH:32]=[CH:31][CH:30]=3)(=[O:26])=[O:25])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1>>[C:12]1([CH:5]([C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:35]2[C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[NH:28][C:27]=2[S:24]([N:18]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)(=[O:25])=[O:26])[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1

Participants

3

Reactant 2

HCID 274281Diphenylmethyl acetateHCID 54554317HCID 54554317, compound

Product 1

HCID 54381562HCID 54381562, compoundYield 81.7%

Procedure

Substantially the same procedure as in Example 263 was repeated using benzhydryl acetate (0.78 g, 3.41 mmol) and 2-(piperidinosulfonyl)indole (0.95 g, 3.59 mmol) to give 1.2 g (yield: 75%) of the title compound.

Sources & evidence

ORD record
ord-32b19fd10857402db193ea80953805cf
Source dataset
uspto-grants-1999_04
Patent number
US05891902

Reaction notes

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