Ammonium Chloride → HCID 57900428, compound

HRID 1949883Notes

Reaction equation

HRID 1949883 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([C:14]2[S:30][C:17]3[C:18]4[CH:26]=[CH:25][C:24]([C:27](O)=[O:28])=[CH:23][C:19]=4[O:20][CH2:21][CH2:22][C:16]=3[CH:15]=2)=[N:12][CH:11]=[N:10]1.[Cl-].[NH4+].C[N:34](C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>C1COCC1>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([C:14]2[S:30][C:17]3[C:18]4[CH:26]=[CH:25][C:24]([C:27]([NH2:34])=[O:28])=[CH:23][C:19]=4[O:20][CH2:21][CH2:22][C:16]=3[CH:15]=2)=[N:12][CH:11]=[N:10]1

Participants

6

Procedure

Following the procedures in Examples 47 and 235, 2-(1-(2,4-difluorophenyl)-1H-1,2,4-triazol-5-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-8-carboxylic acid was reacted with ammonium chloride, HATU and DIPEA in THF to give 328 as a colorless solid after reverse phase HPLC. MS: (ESI+) 425.0

Sources & evidence

ORD record
ord-718a4352b3d34b86b45bc9f981c8331e
Source dataset
uspto-grants-2013_03
Patent number
US08399690B2

Reaction notes

Loading…