HCID 46947722, compound → HCID 87172746, compound

HRID 2370607Notes

Reaction equation

HRID 2370607 reaction equation
[CH3:1][C:2]1([CH3:42])[C:6](=[O:7])[N:5]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:17])[CH3:16])=[C:10]([C:18]([F:21])([F:20])[F:19])[CH:9]=2)[C:4](=[O:22])[N:3]1[CH2:23][CH2:24][O:25][CH2:26][CH2:27][O:28][CH2:29][CH2:30][S:31][CH2:32][CH2:33][CH2:34][C:35]([F:41])([F:40])[C:36]([F:39])([F:38])[F:37].CC1(C)N(CCCCCCCCCSCCCC(F)(F)C(F)(F)F)C(=[O:69])N(C2C=CC([N+]([O-])=O)=C(C(F)(F)F)C=2)C1=O>>[CH3:1][C:2]1([CH3:42])[C:6](=[O:7])[N:5]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:17])[CH3:16])=[C:10]([C:18]([F:20])([F:21])[F:19])[CH:9]=2)[C:4](=[O:22])[N:3]1[CH2:23][CH2:24][O:25][CH2:26][CH2:27][O:28][CH2:29][CH2:30][S:31]([CH2:32][CH2:33][CH2:34][C:35]([F:41])([F:40])[C:36]([F:37])([F:38])[F:39])=[O:69]

Participants

3

Reactant 2

HCID 46947722HCID 46947722, compoundHCID 87134718HCID 87134718, compound

Product 1

HCID 87172746HCID 87172746, compoundYield 75%

Procedure

Compound 39 described below was synthesized according to a similar method to that described in Example 2 using the compound of Example 38 as starting reagent replacing the compound of Example 1. The expected compound is obtained in the form of a pale yellow oil with a yield of 75%.

Workup

  1. custombelow was synthesized

Sources & evidence

ORD record
ord-8a6bb88d3e124dd185064abb7d2ea95a
Source dataset
uspto-grants-2014_04
Patent number
US08710091B2

Reaction notes

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