HCID 15453544, compound → HCID 44337794, compound

HRID 2113049Notes

Reaction equation

HRID 2113049 reaction equation
[CH2:1]([S:8]([NH:11][C:12]1[C:13](=[O:23])[N:14]([CH2:19][C:20]([OH:22])=O)[C:15]([CH3:18])=[CH:16][CH:17]=1)(=[O:10])=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:24][CH2:25][CH:26]1[CH2:35][CH2:34][C:33]2[N:32]=[C:31]([NH2:36])[N:30]=[CH:29][C:28]=2[CH2:27]1>>[NH2:36][C:31]1[N:30]=[CH:29][C:28]2[CH2:27][CH:26]([CH2:25][NH:24][C:20](=[O:22])[CH2:19][N:14]3[C:15]([CH3:18])=[CH:16][CH:17]=[C:12]([NH:11][S:8]([CH2:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)(=[O:9])=[O:10])[C:13]3=[O:23])[CH2:35][CH2:34][C:33]=2[N:32]=1

Participants

3

Reactant 2

HCID 15453544HCID 15453544, compoundHCID 154582213-Benzylsulfonylamino-6-methyl-1-carboxymethyl-2-pyridinone

Product 1

HCID 44337794HCID 44337794, compound

Procedure

The title compound was prepared from 2-[3-[(benzylsulfonyl)amino]-6 -methyl-2-oxo-1(2H)-pyridinyl]acetic acid and 6-(aminomethyl)-5,6,7,8-tetrahydro-2-quinazolinamine using the procedure of EXAMPLE 1 (STEP 6), and was obtained as a white solid compound.

Workup

  1. customwas obtained as a white solid compound

Sources & evidence

ORD record
ord-c0bcf1b8372c49558fdcb74c0c21af31
Source dataset
uspto-grants-2009_04
Patent number
US07524871B2

Reaction notes

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