HCID 117940173, compound → 2-(4-chloro-2-fluorobenzyl)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one

HRID 62235Notes

Reaction equation

HRID 62235 reaction equation
[Cl:1][C:2]1[CH:26]=[CH:25][C:5](/[CH:6]=[C:7]2/[C:8](=[O:24])[C:9]3[C:14]([CH2:15]/2)=[CH:13][C:12]([N:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)=[C:11]([O:22][CH3:23])[CH:10]=3)=[C:4]([F:27])[CH:3]=1>CO.[Pd]>[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([CH2:6][CH:7]2[CH2:15][C:14]3[C:9](=[CH:10][C:11]([O:22][CH3:23])=[C:12]([N:16]4[CH2:21][CH2:20][O:19][CH2:18][CH2:17]4)[CH:13]=3)[C:8]2=[O:24])=[C:4]([F:27])[CH:3]=1

Participants

4

Procedure

Compound 15 (45 mg, 0.121 mmol) was dissolved in methanol and was added Pd/C 20 mg and stirred the reaction under hydrogen balloon for 6 h. The reaction was filtered through celite bed and washed with excess methanol. The organic layer was concentrated to get the crude compound 16. The crude 16 was purified by flash chromatography using 100-200 mesh silica gel. Compound 16 was eluted at 23% ethyl acetate in hexane as half white coloured solid 2-(4-chloro-2-fluorobenzyl)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 16. 1HNMR (400 MHz, CDCl3) δ ppm 7.18 (m, 2H), 6.82 (m, 3H), 3.88 (m, 3H), 3.86 (m, 4H), 3.31 (m, 1H), 3.16 (m, 4H), 3.06 (m, 1H), 2.95 (m, 1H), 2.73 (m, 2H); MS (ESI) m/z 389.8 (M+H).

Workup

  1. customthe reaction under hydrogen balloon for 6 h
  2. filtrationThe reaction was filtered through celite bed
  3. washwashed with excess methanol
  4. concentrationThe organic layer was concentrated

Sources & evidence

ORD record
ord-20570345412345dc9ee7b85c2a6ae078
Source dataset
uspto-grants-2016_09
Patent number
US09446047B2

Reaction notes

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