Oxalyl chloride → HCID 57035411, compound

HRID 397673Notes

Reaction equation

HRID 397673 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH2:15][CH2:14][CH2:13][C@H:12]2[C:16]([NH2:18])=O)(=[O:10])=[O:9])=[CH:4][CH:3]=1.C(Cl)(=O)C(Cl)=O>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([N:11]2[CH2:15][CH2:14][CH2:13][C@H:12]2[C:16]#[N:18])(=[O:10])=[O:9])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 65578Oxalyl chlorideHCID 975442HCID 975442, compound

Product 1

HCID 57035411HCID 57035411, compound

Procedure

The title compound was prepared by a similar method to Preparation 3 from (2S)-1-[(4-fluorophenyl)sulfonyl]-2-pyrrolidinecarboxamide [see Preparation 50] and oxalyl chloride. The crude product was purified by column chromatography on silica gel eluting with dichloromethane to afford (2S)-1-[(4-fluorophenyl)sulfonyl]-2-pyrrolidinecarbonitrile as a white solid.

Workup

  1. customThe crude product was purified by column chromatography on silica gel eluting with dichloromethane

Sources & evidence

ORD record
ord-d8441bc1a298499bb6a89aefc59a963e
Source dataset
uspto-grants-2003_08
Patent number
US06610707B1

Reaction notes

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