1-(Bromomethyl)-2-methanesulfonylbenzene → 7-Chloro-6-(2-methanesulfonylbenzylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine Hydrochloride

HRID 2041398Notes

Reaction equation

HRID 2041398 reaction equation
C(OC([N:8]1[CH2:14][CH2:13][C:12]2[C:15]([S:20][C:21](=O)N(C)C)=[C:16]([Cl:19])[CH:17]=[CH:18][C:11]=2[CH2:10][CH2:9]1)=O)(C)(C)C.BrC[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=1[S:34]([CH3:37])(=[O:36])=[O:35]>>[ClH:19].[Cl:19][C:16]1[CH:17]=[CH:18][C:11]2[CH2:10][CH2:9][NH:8][CH2:14][CH2:13][C:12]=2[C:15]=1[S:20][CH2:21][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=1[S:34]([CH3:37])(=[O:36])=[O:35]

Participants

3

Reactant 2

HCID 189224741-(Bromomethyl)-2-methanesulfonylbenzeneHCID 576559793-tert-butoxycarbonyl-7-chloro-6-dimethylaminocarbonylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Product 1

HCID 667066547-Chloro-6-(2-methanesulfonylbenzylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine Hydrochloride

Procedure

Use a method similar to the Preparation 177, using 3-tert-butoxycarbonyl-7-chloro-6-dimethylcarbamoylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine and 1-bromomethyl-2-methanesulfonyl-benzene to give, after deprotection by the General Procedure 1-4, the title compound and as a white solid. MS (APCI+) m/z: 382 (M+H)+.

Workup

  1. customsimilar to the Preparation 177
  2. customto give

Sources & evidence

ORD record
ord-134515094c5a4983ad6bedebedc27a58
Source dataset
uspto-grants-2013_11
Patent number
US08580780B2

Reaction notes

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