Trifluoroacetic acid → HCID 71553475, compound

HRID 1430216Notes

Reaction equation

HRID 1430216 reaction equation
[CH2:1]([N:8]1[CH:12]=[C:11]([C:13]2[C:14]([C:43]([O:45]C(C)(C)C)=[O:44])=[N:15][C:16]([N:19]3[CH2:28][CH2:27][C:26]4[C:21](=[C:22]([C:29](=[O:42])[NH:30][C:31]5[S:32][C:33]6[CH:39]=[C:38]([F:40])[C:37]([F:41])=[CH:36][C:34]=6[N:35]=5)[CH:23]=[CH:24][CH:25]=4)[CH2:20]3)=[CH:17][CH:18]=2)[CH:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)(C(F)(F)F)=O>ClCCl>[CH2:1]([N:8]1[CH:12]=[C:11]([C:13]2[C:14]([C:43]([OH:45])=[O:44])=[N:15][C:16]([N:19]3[CH2:28][CH2:27][C:26]4[C:21](=[C:22]([C:29](=[O:42])[NH:30][C:31]5[S:32][C:33]6[CH:39]=[C:38]([F:40])[C:37]([F:41])=[CH:36][C:34]=6[N:35]=5)[CH:23]=[CH:24][CH:25]=4)[CH2:20]3)=[CH:17][CH:18]=2)[CH:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

4

Procedure

To a solution of EXAMPLE 7D (0.085 g) in dichloromethane (0.5 mL) was added TFA (0.5 mL) and the reaction was stirred overnight. The reaction mixture was concentrated and dried to provide the title compound. 1H NMR (300 MHz, dimethylsulfoxide-d6) δ ppm 12.98 (s, 1H), 8.20 (dd, 1H), 7.93-7.83 (m, 2H), 7.70 (d, 1H), 7.58 (dd, 2H), 7.47-7.19 (m, 7H), 6.94 (d, 1H), 5.32 (s, 2H), 4.93 (s, 2H), 3.86 (t, 2H), 2.99 (t, 2H).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. customdried

Sources & evidence

ORD record
ord-c6089ae74a8345f6aa023ea32f8c12a7
Source dataset
uspto-grants-2015_01
Patent number
US08940737B2

Reaction notes

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