3-(Trifluoromethyl)phenyl isocyanate → HCID 10121014, compound

HRID 746482Notes

Reaction equation

HRID 746482 reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([N:9]=[C:10]=[O:11])[CH:6]=[CH:7][CH:8]=1.[C:14]1([CH:20]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH2:21][CH2:22][NH:23][CH:24]2[CH2:29][CH2:28][N:27]([C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])[CH2:26][CH2:25]2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>ClCCl>[C:33]([O:32][C:30]([N:27]1[CH2:26][CH2:25][CH:24]([N:23]([CH2:22][CH2:21][CH:20]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[C:10]([NH:9][C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([C:2]([F:12])([F:13])[F:1])[CH:4]=2)=[O:11])[CH2:29][CH2:28]1)=[O:31])([CH3:36])([CH3:34])[CH3:35]

Participants

4

Procedure

246 mg (1.32 mmol) of 3-(trifluoromethyl)phenyl isocyanate is added to a solution of tert-butyl 4-[(3,3-diphenylpropyl)amino]-1-piperidine carboxylate (470 mg, 1.2 mmol) in 5 ml of dichloromethane. The solution is agitated for 45 minutes, and to the aminomethyl resin (180 mg, 0.36 mmol) is added and the reaction medium is again placed on an orbital shaker for 45 minutes. The resin is filtered and washed with dichloromethane. The filtrate is concentrated in vacuo in order to produce 610 mg (yield=87%) of a white foam.

Workup

  1. waitthe reaction medium is again placed on an orbital shaker for 45 minutes
  2. filtrationThe resin is filtered
  3. washwashed with dichloromethane
  4. concentrationThe filtrate is concentrated in vacuo in order

Sources & evidence

ORD record
ord-f888bd0f876a4e61859e3c1a91e8bfc3
Source dataset
uspto-grants-2008_07
Patent number
US07393861B2

Reaction notes

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