Ethylamine → HCID 86680540, compound

HRID 1184621Notes

Reaction equation

HRID 1184621 reaction equation
[F:1][C:2]([F:7])([F:6])[C:3](O)=O.CS(O[CH:13]([C:35]1[CH:40]=C[C:38](C(F)(F)F)=[CH:37][CH:36]=1)[C:14]([N:16]1[CH2:21][CH2:20][N:19]2[CH2:22][C@H:23]([O:25][C:26]3[CH:31]=[N:30][C:29]([CH:32]4[CH2:34][CH2:33]4)=[CH:28][N:27]=3)[CH2:24][C@H:18]2[CH2:17]1)=[O:15])(=O)=O.[F:45][C:46]1([F:51])[CH2:50][CH2:49][NH:48][CH2:47]1.C(N)C>>[CH:32]1([C:29]2[N:30]=[CH:31][C:26]([O:25][C@H:23]3[CH2:22][N:19]4[CH2:20][CH2:21][N:16]([C:14](=[O:15])[CH:13]([N:48]5[CH2:49][CH2:50][C:46]([F:51])([F:45])[CH2:47]5)[C:35]5[CH:36]=[CH:37][CH:38]=[C:3]([C:2]([F:7])([F:6])[F:1])[CH:40]=5)[CH2:17][C@@H:18]4[CH2:24]3)=[N:27][CH:28]=2)[CH2:33][CH2:34]1

Participants

5

Procedure

The title compound was prepared as a trifluoroacetic acid salt according to the procedure described in Example 194B, substituting the product from Example 179A for the product from Example 194A, and substituting 3,3-difluoropyrrolidine for ethylamine. 1H NMR (300 MHz, CDCl3) δ ppm 0.88-1.07 (m, 4 H) 5.37-5.59 (m, 2 H) 7.57-7.73 (m, 3 H) 7.75-7.87 (m, 1 H) 7.89-7.96 (m, 1 H) 7.98-8.12 (m, 1 H); MS (ESI) m/z 552 (M+H)+.

Sources & evidence

ORD record
ord-0da7226ab27841bba6085119690d4ed3
Source dataset
uspto-grants-2014_03
Patent number
US08669255B2

Reaction notes

Loading…