Water → HCID 19829858, compound

HRID 1592054Notes

Reaction equation

HRID 1592054 reaction equation
O.ClS(N=[C:7]=[O:8])(=O)=O.C[Si]([CH:13]([OH:15])[CH3:14])(C)C.[I:16][C:17]1[CH:18]=[C:19]([CH:21]=[CH:22][CH:23]=1)[NH2:20]>C(Cl)Cl>[CH3:7][O:8][C:13](=[O:15])[CH2:14][NH:20][C:19]1[CH:21]=[CH:22][CH:23]=[C:17]([I:16])[CH:18]=1

Participants

6

Reactant 4

HCID 962WaterHCID 122713-IodoanilineHCID 70918Chlorosulfonyl isocyanateHCID 124478981-(Trimethylsilyl)ethanol

Product 1

HCID 19829858HCID 19829858, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a cooled (ice/salt/water bath) solution of chlorosulfonylisocyanate (3.23 mL, 37.1 mmol) in CH2Cl2 (100 mL) is added trimethylsilylethanol (5.32 mL, 37.1 mmol). After 1 h, a solution of (3-Iodo-phenylamino)-acetic acid methyl ester (2.7 g, 9.28 mmol) (obtained by alkylation of 3-iodoaniline using the method of Tohru Fukuyama et. al., Tett. Lett. 38 (33) pp. 5831-34,1997) and TEA (5.3 mL, 38.04 mmol) in CH2Cl2 (50 mL) is added and the reaction is stirred for 2.5 h. The mixture is poured into 400 mL of 1N aqueous HCl and extracted with EtOAc. The EtOAc layer is washed with 1N aqueous HCl, dried over anhydrous Na2SO4, filtered and concentrated. Chromatography on a 110 g silica gel RediSep (Isco Inc.) column with a 30 mL/min gradient elution of 10:90 (EtOAc:hexane) to 40:60 over 55 min gives an oil. Trituration with Et2O yields N-(2-trimethylsilylethoxycarbonyl-sulfamoyl)-N-(3-iodo-phenyl)glycine methyl ester as a white solid.

Sources & evidence

ORD record
ord-25c2cf4a48d24cae9d91425ad0bae74e
Source dataset
uspto-grants-2007_11
Patent number
US07291635B2

Reaction notes

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