Ammonium Chloride → HCID 57955598, compound

HRID 1880883Notes

Reaction equation

HRID 1880883 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]1

Participants

4

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

  1. customas described in the General procedure for amide bond synthesis
  2. customThe final compound was purified by reverse phase HPLC
  3. 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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