Benzenesulfonyl chloride → HCID 68278827, compound

HRID 1506914Notes

Reaction equation

HRID 1506914 reaction equation
[C:1]1([S:7]([NH:10][C:11]2[S:15][C:14]3[CH2:16][CH2:17][CH2:18][CH2:19][C:13]=3[C:12]=2[C:20]([O:22][CH2:23]C)=[O:21])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N[C:26]1SC(CC)=C(C(C)C)C=1C(OC)=O.C1(S(Cl)(=O)=O)C=CC=CC=1>>[C:1]1([S:7]([NH:10][C:11]2[S:15][C:14]([CH2:16][CH3:17])=[C:13]([CH:19]([CH3:26])[CH3:18])[C:12]=2[C:20]([O:22][CH3:23])=[O:21])(=[O:8])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

4

Reactant 3

HCID 7369Benzenesulfonyl chlorideHCID 391240Ethyl 2-(benzenesulfonamido)-4,5,6,7-tetrahydrobenzothiophene-3-carboxylateHCID 68278837HCID 68278837, compound2×

Product 1

HCID 68278827HCID 68278827, compound

Procedure

Prepared by proceeding in a similar manner to Intermediate 1, starting from methyl 2-amino-5-ethyl-4-isopropylthiophene-3-carboxylate (Intermediate 25) and benzenesulphonyl chloride

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-f0371c718abe4bee876cd9ddd6d40aef
Source dataset
uspto-grants-2015_12
Patent number
US09221787B2

Reaction notes

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