Piperidine → HCID 178525540, compound

HRID 867318Notes

Reaction equation

HRID 867318 reaction equation
C1CCNCC1.O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(Br)cc(F)cc21>CS(C)=O.O=C(O)C(=O)Nc1c(F)cccc1S(=O)(=O)N1CCCCC1.O=P([O-])([O-])[O-].[Cu][I].[K+].[K+].[K+]>O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21

Participants

7

Reactant 2

HCID 8082PiperidineHCID 11597294(R)-2-(5-broMo-4-(4-chlorobenzyl)-7-fluoro-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid

Product 1

HCID 178525540HCID 178525540, compoundYield 0%

Reagents, catalysts & solvents 4

HCID 62657Potassium Phosphate, TribasicReagentHCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 1242030262-Fluoro-6-(piperidine-1-sulfonyl)anilino(oxo)acetic acidCatalystHCID 679Dimethyl SulfoxideSolvent2×

Conditions

Temperature
80 °C

Workup

  1. additionThe reaction vials were then cooled to r.t. and diluted with 100 μL of 5% AcOH in DMSO, containing 1,3,5-trimethoxybenzene (0.005M) and were shaken vigorously.
  2. aliquot25 microliter of resulting solution is taken
  3. additionTo the 25 microliter aliquot 700 microliter of MeCN was added prior to UPLC-MS Analysis

Sources & evidence

ORD record
ord-25f4511e384a4be59c632e62f0425ebc
Source dataset
Figure 4 from Chemistry informer libraries
Original link
View source

Reaction notes

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