Diisopropylthiourea → 4-(3,4-Dichloro-5-sulfamoylphenyl)-3-isopropyl-2-isopropylimino-1,3-thiazolidine-4-ol-hydrochloride

HRID 460816Notes

Reaction equation

HRID 460816 reaction equation
[Cl:1][CH2:2][C:3]([C:5]1[CH:10]=[C:9]([S:11](=[O:14])(=[O:13])[NH2:12])[C:8]([Cl:15])=[C:7]([Cl:16])[CH:6]=1)=[O:4].[CH:17]([NH:20][C:21]([NH:23][CH:24]([CH3:26])[CH3:25])=[S:22])([CH3:19])[CH3:18]>>[ClH:1].[Cl:16][C:7]1[CH:6]=[C:5]([C:3]2([OH:4])[CH2:2][S:22][C:21](=[N:20][CH:17]([CH3:19])[CH3:18])[N:23]2[CH:24]([CH3:26])[CH3:25])[CH:10]=[C:9]([S:11](=[O:14])(=[O:13])[NH2:12])[C:8]=1[Cl:15]

Participants

3

Reactant 2

HCID 2758386DiisopropylthioureaHCID 227564452,3',4'-Trichloro-5'-sulfamoylacetophenone

Product 1

HCID 213948004-(3,4-Dichloro-5-sulfamoylphenyl)-3-isopropyl-2-isopropylimino-1,3-thiazolidine-4-ol-hydrochloride

Procedure

was obtained in a manner analogous to the method described in Example 1 d from 6.1 g of 2,3',4'-trichloro-5'-sulfamoylacetophenone and 1,3-diisopropyl-thiourea. M.p. 171° C (decomposition).

Workup

  1. customwas obtained in a manner analogous to the method

Sources & evidence

ORD record
ord-ab9cf720bf984a7985a4cda0837d90e1
Source dataset
uspto-grants-1977_12
Patent number
US04061647

Reaction notes

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