3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride) → HCID 68581305, compound

HRID 2237477Notes

Reaction equation

HRID 2237477 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][C:9]2[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=2[NH:7][S:6]1(=[O:16])=[O:15].[Cl:17][C:18]1[CH:19]=[C:20](B(O)O)[CH:21]=[CH:22][C:23]=1[F:24]>>[Cl:17][C:18]1[CH:19]=[C:20]([N:7]2[C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[CH2:10][N:5]([CH2:4][CH2:3][CH2:2][Cl:1])[S:6]2(=[O:16])=[O:15])[CH:21]=[CH:22][C:23]=1[F:24]

Participants

3

Procedure

In an analogous manner to Example 1 step 7, 3-(3-chloropropyl)-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxide (522 mg) was coupled to 3-chloro-4-fluorophenylboronic acid to provide 1-(3-chloro-4-fluorophenyl)-3-(3-chloropropyl)-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxide (138 mg):

Sources & evidence

ORD record
ord-0f505f546598492b9cd3fcde007931b3
Source dataset
uspto-grants-2010_05
Patent number
US07718652B2

Reaction notes

Loading…