N-(4-Bromobutyl)phthalimide → HCID 9980269, compound

HRID 1655979Notes

Reaction equation

HRID 1655979 reaction equation
[CH2:1]([NH:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[O:7][CH:6]1OC)[CH2:2][CH3:3].BrCCCCN1[C:26](=[O:27])C2=CC=CC=C2C1=O.Br[CH2:34][CH2:35][CH2:36][NH:37][S:38]([C:41]1[CH:46]=[CH:45][C:44]([CH3:47])=[CH:43][CH:42]=1)(=[O:40])=[O:39]>>[CH3:26][O:27][C:12]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:13]=1[CH2:14][CH:5]([N:4]([CH2:1][CH2:2][CH3:3])[CH2:34][CH2:35][CH2:36][NH:37][S:38]([C:41]1[CH:46]=[CH:45][C:44]([CH3:47])=[CH:43][CH:42]=1)(=[O:40])=[O:39])[CH2:6][O:7]2

Participants

4

Reactant 3

HCID 93575N-(4-Bromobutyl)phthalimideHCID 11380772N-(p-toluenesulfonyl)-3-bromopropylamineHCID 19789741HCID 19789741, compound

Product 1

HCID 9980269HCID 9980269, compoundYield 65%

Procedure

Using the procedure described in Example 1, but replacing 3-amino-5-methoxychroman by 3-(N-propylamino)-methoxychroman and N-(4-bromobutyl)phthalimide by -bromo-3-(4-toluenesulfonylamino)propane, and leaving stirring for 72 hours, the expected product is obtained.

Workup

  1. customleaving

Sources & evidence

ORD record
ord-968fbe5884d747e8adae544a76607cb5
Source dataset
uspto-grants-1993_10
Patent number
US05252578

Reaction notes

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