Azetidine → HCID 22314121, compound

HRID 347064Notes

Reaction equation

HRID 347064 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:22]=[CH:21][C:10]2[C:11]([C:14]3[CH:19]=[CH:18][C:17]([Br:20])=[CH:16][CH:15]=3)=[N:12][S:13][C:9]=2[CH:8]=1.[NH:23]1[CH2:26][CH2:25][CH2:24]1>>[N:23]1([CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]2[CH:22]=[CH:21][C:10]3[C:11]([C:14]4[CH:19]=[CH:18][C:17]([Br:20])=[CH:16][CH:15]=4)=[N:12][S:13][C:9]=3[CH:8]=2)[CH2:26][CH2:25][CH2:24]1

Participants

3

Reactant 2

HCID 10422AzetidineHCID 22313931HCID 22313931, compound

Product 1

HCID 22314121HCID 22314121, compound

Procedure

According to the method in example 4, 6-(4-Bromo-butoxy)-3-(4-bromo-phenyl)-benzo[d]isothiazole and azetidine were converted to yield 6-(4-Azetidin-1-yl-butoxy)-3-(4-bromo-phenyl)-benzo[d]isothiazole, MS: 418 (MH+, 1Br).

Sources & evidence

ORD record
ord-36c9f6ad4edc4d3aa17c2a7087f9b402
Source dataset
uspto-grants-2007_02
Patent number
US07173043B2

Reaction notes

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