HCID 90419042, compound → HCID 90419005, compound

HRID 514856Notes

Reaction equation

HRID 514856 reaction equation
[F:1][C:2]1[C:7]2=[N:8]S[N:10]=[C:6]2[C:5]([S:11]([NH:14][C:15]2[CH:25]=[CH:24][C:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:17][CH:16]=2)(=[O:13])=[O:12])=[CH:4][CH:3]=1>CC(O)=O.O.[Zn]>[NH2:10][C:6]1[C:7]([NH2:8])=[C:2]([F:1])[CH:3]=[CH:4][C:5]=1[S:11]([NH:14][C:15]1[CH:25]=[CH:24][C:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:17][CH:16]=1)(=[O:12])=[O:13]

Participants

4

Conditions

Temperature
70 °C

Procedure

To a solution of the compound 39D (382 mg, 1.0 mmol) in AcOH/H2O (8 mL/3 mL) at 70° C. was added zinc powder (975 mg, 15 mmol) and the resulting suspension was stirred at 70° C. for 1 h. The solid was filtered off and washed with EtOAc. The filtrate was partitioned between satd. NaHCO3 and EtOAc. The organic layer was separated and washed with water and brine, dried over anhydrous Na2SO4 and concentrated to give crude product 39E, which was confirmed by LCMS, and used in the next reaction without further purification. LC-MS: m/z 354.4 (M+H)+.

Workup

  1. filtrationThe solid was filtered off
  2. washwashed with EtOAc
  3. customThe filtrate was partitioned between satd
  4. customThe organic layer was separated
  5. washwashed with water and brine
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-0582c8ca31514882b5cf5015f4520423
Source dataset
uspto-grants-2015_08
Patent number
US09108921B2

Reaction notes

Loading…