2-[4-(2-hydroxyethyl)piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide → 2-[4-[2-(5-chloro-7-isopropyl-4-methylbenzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(pyrrolidin-1-yl)-6-methylpyridin-3-yl]acetamide

HRID 227533Notes

Reaction equation

HRID 227533 reaction equation
OCCN1CCN(CC(NC2C(SC)=NC(C)=CC=2SC)=O)CC1.O[CH2:26][CH2:27][N:28]1[CH2:33][CH2:32][N:31]([CH2:34][C:35]([NH:37][C:38]2[C:39]([N:50]3[CH2:54][CH2:53][CH2:52][CH2:51]3)=[N:40][C:41]([CH3:49])=[CH:42][C:43]=2[N:44]2[CH2:48][CH2:47][CH2:46][CH2:45]2)=[O:36])[CH2:30][CH2:29]1.SC1NC2C=CC=CC=2N=1.[SH:65][C:66]1[O:67][C:68]2[C:74]([CH:75]([CH3:77])[CH3:76])=[CH:73][C:72]([Cl:78])=[C:71]([CH3:79])[C:69]=2[N:70]=1>>[Cl:78][C:72]1[CH:73]=[C:74]([CH:75]([CH3:76])[CH3:77])[C:68]2[O:67][C:66]([S:65][CH2:26][CH2:27][N:28]3[CH2:29][CH2:30][N:31]([CH2:34][C:35]([NH:37][C:38]4[C:39]([N:50]5[CH2:51][CH2:52][CH2:53][CH2:54]5)=[N:40][C:41]([CH3:49])=[CH:42][C:43]=4[N:44]4[CH2:45][CH2:46][CH2:47][CH2:48]4)=[O:36])[CH2:32][CH2:33]3)=[N:70][C:69]=2[C:71]=1[CH3:79]

Participants

5

Reactant 4

HCID 116892402-[4-(2-hydroxyethyl)piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamideHCID 210873432-[4-(2-hydroxyethyl)piperazin-1-yl]-N-[2,4-bis(pyrrolidin-1-yl)-6-methylpyridin-3-yl]acetamideHCID 178427920HCID 178427920, compoundHCID 178527775HCID 178527775, compound

Product 1

HCID 210873292-[4-[2-(5-chloro-7-isopropyl-4-methylbenzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(pyrrolidin-1-yl)-6-methylpyridin-3-yl]acetamide

Procedure

The reaction and treatments of Example 12 were repeated, except that 2-[4-(2-hydroxyethyl)piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methylpyridin-3-yl]acetamide was replaced by 2-[4-(2-hydroxyethyl)piperazin-1-yl]-N-[2,4-bis(pyrrolidin-1-yl)-6-methyl-3-pyridyl]acetamide, and 2-mercaptobenzimidazole was replaced by 2-mercapto-5-chloro-7-isopropyl-4-methylbenzoxazole, to thereby yield the title compound as a pale yellow oil.

Workup

  1. customThe reaction and treatments of Example 12

Sources & evidence

ORD record
ord-a8f4dce33336497aaba7ed85959c3b9c
Source dataset
uspto-grants-2009_07
Patent number
US07560547B2

Reaction notes

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