HCID 23144087, compound → HCID 23144278, compound

HRID 337454Notes

Reaction equation

HRID 337454 reaction equation
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([NH:19][C:20]([C:22]2[CH:27]=[CH:26][N:25]=[C:24]([O:28]CC3C=CC(OC)=CC=3)[CH:23]=2)=[O:21])[S:9][C:10]=1[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=1)=[O:12]>FC(F)(F)C(O)=O>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([NH:19][C:20]([C:22]2[CH:27]=[CH:26][NH:25][C:24](=[O:28])[CH:23]=2)=[O:21])[S:9][C:10]=1[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=1)=[O:12]

Participants

3

Procedure

Compound 213 (912 mg, 1.78 mmol) was dissolved in trifluoroacetic acid (3.6 mL), followed by stirring at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the resulting residue was reslurried with ethyl acetate to afford the entitled Compound 231 (469 mg, 67%) as a pale yellow solid.

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure

Sources & evidence

ORD record
ord-dae92682fe9d4c1ba192dad3cf839213
Source dataset
uspto-grants-2014_11
Patent number
US08889718B2

Reaction notes

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