3-Phenylpropylamine → (3-Phenyl-n-propyl)aminosulfonylacetonitrile

HRID 1976197Notes

Reaction equation

[C:1]1([CH2:7][CH2:8][CH2:9][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:11]([CH2:13][S:14](Cl)(=[O:16])=[O:15])#[N:12].C(NS(CC#N)(=O)=O)C1C=CC=CC=1>>[C:1]1([CH2:7][CH2:8][CH2:9][NH:10][S:14]([CH2:13][C:11]#[N:12])(=[O:16])=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

Reactant 3

HCID 162593-Phenylpropylamine

HCID 13142426Cyanomethanesulfonyl chloride

HCID 15410493HCID 15410493, compound

Product 1

HCID 15410494(3-Phenyl-n-propyl)aminosulfonylacetonitrile

Procedure

N-3-Phenyl-n-propyl cyanomethylsulfonamide was prepared with 3-phenyl-n-propylamine and cyanomethylsulphonyl chloride under the similar conditions as described for N-benzyl cyanomethylsulfonamide (Part A, EXAMPLE 12).

Sources & evidence

ORD record: ord-d60e814684774749a55b584c597e3979
Source dataset: uspto-grants-2001_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06225346B1

Reaction notes

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