N-(2-Aminoethyl)methanesulfonamide → HCID 22671274, compound

HRID 1097336Notes

Reaction equation

HRID 1097336 reaction equation
Cl[C:2]1[C:3]2[S:20][C:19]([NH2:21])=[N:18][C:4]=2[N:5]=[C:6]([S:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[C:11]=2[F:17])[N:7]=1.[NH2:22][CH2:23][CH2:24][NH:25][S:26]([CH3:29])(=[O:28])=[O:27]>>[NH2:21][C:19]1[S:20][C:3]2[C:2]([NH:22][CH2:23][CH2:24][NH:25][S:26]([CH3:29])(=[O:28])=[O:27])=[N:7][C:6]([S:8][CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[C:11]=3[F:17])=[N:5][C:4]=2[N:18]=1

Participants

3

Reactant 2

HCID 533845N-(2-Aminoethyl)methanesulfonamideHCID 112216507-Chloro-5-[[(2,3-difluorophenyl)methyl]thio]-thiazolo[4,5-d]pyrimidin-2-amine

Product 1

HCID 22671274HCID 22671274, compound

Procedure

Prepared by the method of example 2 step a), using the product of example 4, step b) and N-[2-aminoethyl]-methanesulfonamide,

Workup

  1. customPrepared by the method of example 2 step a),

Sources & evidence

ORD record
ord-d36d9543683b44e1b0208a3314974775
Source dataset
uspto-grants-2012_03
Patent number
US08143261B2

Reaction notes

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