Hydrochloric Acid → 2-Amino-pyrimidine-5-carboxylic acid [1-(2-p-tolyl-ethanesulfonyl)-piperidin-4-ylmethyl]-amide

HRID 854314Notes

Reaction equation

HRID 854314 reaction equation
[C:1]1([CH3:20])[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][S:9]([N:12]2[CH2:17][CH2:16][CH:15]([CH2:18][NH2:19])[CH2:14][CH2:13]2)(=[O:11])=[O:10])=[CH:3][CH:2]=1.C(OC([NH:28][C:29]1[N:34]=[CH:33][C:32]([C:35](O)=[O:36])=[CH:31][N:30]=1)=O)(C)(C)C.Cl>O1CCOCC1>[C:1]1([CH3:20])[CH:2]=[CH:3][C:4]([CH2:7][CH2:8][S:9]([N:12]2[CH2:17][CH2:16][CH:15]([CH2:18][NH:19][C:35]([C:32]3[CH:31]=[N:30][C:29]([NH2:28])=[N:34][CH:33]=3)=[O:36])[CH2:14][CH2:13]2)(=[O:10])=[O:11])=[CH:5][CH:6]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 21471626HCID 21471626, compoundHCID 69418130C-[1-(2-p-tolyl-ethanesulfonyl)-piperidin-4-yl]-methylamine

Product 1

HCID 589334272-Amino-pyrimidine-5-carboxylic acid [1-(2-p-tolyl-ethanesulfonyl)-piperidin-4-ylmethyl]-amide

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

The title compound was prepared from C-[1-(2-p-tolyl-ethanesulfonyl)-piperidin-4-yl]-methylamine and 2-tert-butoxycarbonylamino-pyrimidine-5-carboxylic acid, followed by treatment with 4N HCl in dioxane as described in EXAMPLE 192.

Sources & evidence

ORD record
ord-8a7e80f6fe31414cb3a80dbbd5aeb8fa
Source dataset
uspto-grants-2007_08
Patent number
US07259157B2

Reaction notes

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