Sodium Iodide → HCID 59003313, compound

HRID 2267560Notes

Reaction equation

HRID 2267560 reaction equation
Cl[CH2:2][CH2:3][CH2:4][S:5]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:22]3[C:17](=[C:18]([C:29]([NH2:31])=[O:30])[CH:19]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[CH:21]=3)[NH:16][CH:15]=2)[CH2:10][CH2:9]1)(=[O:7])=[O:6].[O:32]1[CH2:36][CH2:35][CH:34]([CH2:37][OH:38])[CH2:33]1.C([O-])([O-])=O.[K+].[K+].[I-].[Na+]>>[C:23]1([C:20]2[CH:21]=[C:22]3[C:17](=[C:18]([C:29]([NH2:31])=[O:30])[CH:19]=2)[NH:16][CH:15]=[C:14]3[CH:11]2[CH2:12][CH2:13][N:8]([S:5]([CH2:4][CH2:3][CH2:2][O:38][CH2:37][CH:34]3[CH2:35][CH2:36][O:32][CH2:33]3)(=[O:7])=[O:6])[CH2:9][CH2:10]2)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

Participants

5

Reactant 4

HCID 5238Sodium IodideHCID 11430Potassium CarbonateHCID 139980Tetrahydro-3-furanmethanolHCID 590032803-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide

Product 1

HCID 59003313HCID 59003313, compoundYield 15.3%

Procedure

Following the general procedure of example 159, 3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide (40.0 mg, 0.087 mmol), tetrahydro-3-furanylmethanol (102 mg, 0.87 mmol), K2CO3 (35.0 mg, 0.35 mmol) and sodium iodide (0.5 mg) were reacted to give the title compound (7.0 mg, 15.3%).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-dfdb0763339548619af43b2beb78aa5d
Source dataset
uspto-grants-2010_12
Patent number
US07858796B2

Reaction notes

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