Diisopropylethylamine → HCID 25234394, compound

HRID 1665036Notes

Reaction equation

HRID 1665036 reaction equation
[CH2:1]([NH:5][CH2:6][C:7]1[S:8][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([S:18]([CH3:21])(=[O:20])=[O:19])[CH:13]=2)=[CH:10][CH:11]=1)[CH:2]([CH3:4])[CH3:3].[Cl:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([Cl:29])[C:24]=1[S:30](Cl)(=[O:32])=[O:31].C(N(CC)C(C)C)(C)C>ClCCl>[Cl:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([Cl:29])[C:24]=1[S:30]([N:5]([CH2:1][CH:2]([CH3:4])[CH3:3])[CH2:6][C:7]1[S:8][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([S:18]([CH3:21])(=[O:20])=[O:19])[CH:13]=2)=[CH:10][CH:11]=1)(=[O:32])=[O:31]

Participants

5

Reactant 3

HCID 81531DiisopropylethylamineHCID 5221832,6-DichlorobenzenesulfonylchlorideHCID 67441398Isobutyl-[5-(3-methanesulfonyl-phenyl)-thiophen-2-ylmethyl]-amine

Product 1

HCID 25234394HCID 25234394, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

In analogy to example 13, step 2, isobutyl-[5-(3-methanesulfonyl-phenyl)-thiophen-2-ylmethyl]-amine (example 15, step 2) was reacted with 2,6-dichlorophenylsulfonyl chloride in presence of N,N-diisopropyl ethyl amine in dichloromethane to give 2,6-dichloro-N-isobutyl-N-[5-(3-methanesulfonyl-phenyl)-thiophen-2-ylmethyl]-benzenesulfonamide as a colorless oil. MS: 549.3 ([M+NH4]+)

Sources & evidence

ORD record
ord-899f3248c68543a68283ff12c84108a3
Source dataset
uspto-grants-2011_10
Patent number
US08039493B2

Reaction notes

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