3-(methylsulfonyl)pyrrolidine → HCID 66834511, compound

HRID 61741Notes

Reaction equation

HRID 61741 reaction equation
[C:1]([C:3]1[CH:15]=[C:14]2[C:6]([C:7]3[C:8](=[O:30])[C:9]4[CH:21]=[CH:20][C:19](OS(C(F)(F)F)(=O)=O)=[CH:18][C:10]=4[C:11]([CH3:17])([CH3:16])[C:12]=3[NH:13]2)=[CH:5][CH:4]=1)#[N:2].[CH3:31][S:32]([CH:35]1[CH2:39][CH2:38][NH:37][CH2:36]1)(=[O:34])=[O:33]>>[CH3:31][S:32]([CH:35]1[CH2:39][CH2:38][N:37]([C:19]2[CH:20]=[CH:21][C:9]3[C:8](=[O:30])[C:7]4[C:6]5[C:14](=[CH:15][C:3]([C:1]#[N:2])=[CH:4][CH:5]=5)[NH:13][C:12]=4[C:11]([CH3:17])([CH3:16])[C:10]=3[CH:18]=2)[CH2:36]1)(=[O:34])=[O:33]

Participants

3

Reactant 2

HCID 34193563-(methylsulfonyl)pyrrolidineHCID 86663817Trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl ester

Product 1

HCID 66834511HCID 66834511, compound

Procedure

Under the same conditions as the method for synthesizing Compound B2-1, the title compound was prepared from Compound B1 and 3-methanesulfonylpyrrolidine.

Workup

  1. customUnder the same conditions as the method for synthesizing Compound B2-1

Sources & evidence

ORD record
ord-bfb27509047941b6a86a48492974b1df
Source dataset
uspto-grants-2016_09
Patent number
US09440922B2

Reaction notes

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