1-Iodo-3-methylbutane → HCID 46890089, compound

HRID 1453710Notes

Reaction equation

HRID 1453710 reaction equation
C([O:5][C:6](=[O:29])[CH2:7][N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([CH:17]2[C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=3[S:19](=[O:27])(=[O:26])[NH:18]2)=[C:9]1[CH3:28])(C)(C)C.I[CH2:31][CH2:32][CH:33]([CH3:35])[CH3:34]>>[CH3:28][C:9]1[N:8]([CH2:7][C:6]([OH:5])=[O:29])[C:16]2[C:11]([C:10]=1[CH:17]1[C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=3[S:19](=[O:26])(=[O:27])[N:18]1[CH2:31][CH2:32][CH:33]([CH3:35])[CH3:34])=[CH:12][CH:13]=[CH:14][CH:15]=2

Participants

3

Reactant 2

HCID 109241-Iodo-3-methylbutaneHCID 67317115[3-(1,1-Dioxo-2,3-dihydro-1h-1lambda6-benzo[d]isothiazol-3-yl)-2-methyl-indol-1-yl]-acetic acid tert-butyl ester

Product 1

HCID 46890089HCID 46890089, compound

Procedure

The title compound was prepared by the method described for example 14 using the product from example 3, step c) and 1-iodo-3-methyl-butane. MS: ESI (negative): 425 (M−H).

Sources & evidence

ORD record
ord-0be9ffccdd5042038de2838aea5d23e2
Source dataset
uspto-grants-2009_01
Patent number
US07476667B2

Reaction notes

Loading…