Dipropylamine → N-{[7-(Methylsulfonyl)-3,4-dihydro-2H-chromen-2-YL]methyl}-N-propylpropan-1-amine

HRID 38967Notes

Reaction equation

HRID 38967 reaction equation
CC1C=CC(S(O[CH2:12][CH:13]2[CH2:22][CH2:21][C:20]3[C:15](=[CH:16][C:17]([S:23]([CH3:26])(=[O:25])=[O:24])=[CH:18][CH:19]=3)[O:14]2)(=O)=O)=CC=1.[CH2:27]([NH:30][CH2:31][CH2:32][CH3:33])[CH2:28][CH3:29]>C(#N)C>[CH3:26][S:23]([C:17]1[CH:16]=[C:15]2[C:20]([CH2:21][CH2:22][CH:13]([CH2:12][N:30]([CH2:31][CH2:32][CH3:33])[CH2:27][CH2:28][CH3:29])[O:14]2)=[CH:19][CH:18]=1)(=[O:24])=[O:25]

Participants

4

Reactant 2

HCID 8902DipropylamineHCID 86652940[7-(methylsulfonyl)-3,4-dihydro-2H-chromen-2-yl]methyl 4-methylbenzenesulfonate

Product 1

HCID 44468513N-{[7-(Methylsulfonyl)-3,4-dihydro-2H-chromen-2-YL]methyl}-N-propylpropan-1-amine

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Preparation according to Example 25: [7-(methylsulfonyl)-3,4-dihydro-2H-chromen-2-yl]methyl 4-methylbenzenesulfonate (0.020 g, 0.0504 mmol), N-propylpropan-1-amine (0.5 ml), ACN (3 ml). MS m/z (rel. intensity, 70 eV) 325 (M+, 1), 296 (7), 131 (4), 115 (10), 114 (bp), 86 (6).

Workup

  1. customPreparation

Sources & evidence

ORD record
ord-115a309523ce46fd8dc9390864734267
Source dataset
uspto-grants-2013_09
Patent number
US08524766B2

Reaction notes

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