Methylamine → HCID 57886343, compound

HRID 1818858Notes

Reaction equation

HRID 1818858 reaction equation
Br[CH2:2][CH2:3][O:4][CH2:5][CH2:6][N:7]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[N:9]([C:16]2[C:21]([F:22])=[CH:20][CH:19]=[CH:18][C:17]=2[F:23])[S:8]1(=[O:25])=[O:24].[CH3:26][NH2:27]>CO>[F:23][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]([F:22])[C:16]=1[N:9]1[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[N:7]([CH2:6][CH2:5][O:4][CH2:3][CH2:2][NH:27][CH3:26])[S:8]1(=[O:25])=[O:24]

Participants

4

Procedure

In an analogous manner to general procedure V, 1-[2-(2-bromoethoxy)ethyl]-3-(2,6-difluorophenyl)-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide (0.1 g, 0.23 mmol) was treated with 8N methylamine in methanol to give 2-{2-[3-(2,6-difluorophenyl)-2,2-dioxido-2,1,3-benzothiadiazol-1(3H)-yl]ethoxy}-N-methylethanamine which was treated with 1N hydrochloric acid in ether to give its hydrochloride salt as a white solid (0.24 g, 25%). HRMS: calcd for C17H19F2N3O3S+H+, 384.11879; found (ESI, [M+H]+Obs'd), 384.1184.

Sources & evidence

ORD record
ord-0cf8396b07404cada253e06f2c1dc2b1
Source dataset
uspto-grants-2009_10
Patent number
US07601722B2

Reaction notes

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