Ammonium Chloride → HCID 57955598, compound
Reaction equation
[CH:1]1([N:7]2[CH2:13][C:12]([F:15])([F:14])[C:11](=[O:16])[N:10]([CH3:17])[C:9]3[CH:18]=[N:19][C:20]([NH:22][C:23]4[CH:31]=[CH:30][C:26]([C:27](O)=[O:28])=[CH:25][C:24]=4[O:32][CH3:33])=[N:21][C:8]2=3)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C[N:35](C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[Cl-].[NH4+]>>[CH:1]1([N:7]2[CH2:13][C:12]([F:14])([F:15])[C:11](=[O:16])[N:10]([CH3:17])[C:9]3[CH:18]=[N:19][C:20]([NH:22][C:23]4[CH:31]=[CH:30][C:26]([C:27]([NH2:35])=[O:28])=[CH:25][C:24]=4[O:32][CH3:33])=[N:21][C:8]2=3)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 3
Product 1
Procedure
The title compound was synthesized from 4-(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[5,4-b][1,4]diazepin-2-ylamino)-3-methoxybenzoic acid as described in the General procedure for amide bond synthesis using HATU and ammonium chloride. The final compound was purified by reverse phase HPLC and basified to give the free base. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.10-1.41 (m, 3 H) 1.54-1.86 (m, 7 H) 3.32 (s, 3 H) 3.93 (s, 3 H) 4.17 (t, J=12.5 Hz, 2 H) 4.44-4.55 (m, 1 H) 7.33 (s, 1 H) 7.55 (d, J=8.3 Hz, 1 H) 7.59 (s, 1 H) 7.99 (s, 1 H) 8.13 (d, J=8.1 Hz, 1 H) 8.24 (s, 1 H) 8.61 (s, 1 H). [M+H] calc'd for C22H26F2N6O3 461; found 461.
Workup
- customas described in the General procedure for amide bond synthesis
- customThe final compound was purified by reverse phase HPLC
- customto give the free base
Sources & evidence
- ORD record
- ord-ce6bb8d4f2c44cc39f243060e2c2a1d4
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318727B2
Reaction notes
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