Sodium Iodide → HCID 86758800, compound

HRID 1634821Notes

Reaction equation

HRID 1634821 reaction equation
[CH3:1][O:2][C:3](=[O:38])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][NH:13][C:14]([NH:16][C:17]2[CH:22]=[CH:21][C:20]([S:23]([N:26]3[CH2:31][CH2:30][CH:29]([CH:32](OC)[O:33]C)[CH2:28][CH2:27]3)(=[O:25])=[O:24])=[CH:19][CH:18]=2)=[O:15])=[C:8]([F:37])[CH:7]=1.[I-].[Na+].ClC([SiH3])(Cl)Cl>>[CH3:1][O:2][C:3](=[O:38])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][NH:13][C:14]([NH:16][C:17]2[CH:18]=[CH:19][C:20]([S:23]([N:26]3[CH2:31][CH2:30][CH:29]([CH:32]=[O:33])[CH2:28][CH2:27]3)(=[O:24])=[O:25])=[CH:21][CH:22]=2)=[O:15])=[C:8]([F:37])[CH:7]=1

Participants

4

Procedure

The title compound was prepared from (4-{3-[4-(4-dimethoxymethyl-piperidine-1-sulfonyl)-phenyl]-ureidomethyl}-3-fluoro-phenoxy)-acetic acid methyl ester (0.274 g, 0.5 mmol), sodium iodide (0.185 g, 1.2 mmol), and trichloromethylsilane (0.118 mL, 1.0 mmol) according to the procedure used for example 84 (Step D) and used directly in the next step

Sources & evidence

ORD record
ord-22ce44038bf84ced897144c3d62b7909
Source dataset
uspto-grants-2003_01
Patent number
US06506901B2

Reaction notes

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