1-(Cyclopropylmethyl)piperazine → HCID 57955515, compound

HRID 914211Notes

Reaction equation

HRID 914211 reaction equation
[CH:1]1([N:6]2[CH2:12][C:11]([F:14])([F:13])[C:10](=[O:15])[N:9]([CH3:16])[C:8]3[CH:17]=[N:18][C:19]([NH:21][C:22]4[CH:30]=[CH:29][C:25]([C:26](O)=[O:27])=[CH:24][C:23]=4[O:31][CH3:32])=[N:20][C:7]2=3)[CH2:5][CH2:4][CH2:3][CH2:2]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH:57]1([CH2:60][N:61]2[CH2:66][CH2:65][NH:64][CH2:63][CH2:62]2)[CH2:59][CH2:58]1>>[CH:1]1([N:6]2[CH2:12][C:11]([F:13])([F:14])[C:10](=[O:15])[N:9]([CH3:16])[C:8]3[CH:17]=[N:18][C:19]([NH:21][C:22]4[CH:30]=[CH:29][C:25]([C:26]([N:64]5[CH2:65][CH2:66][N:61]([CH2:60][CH:57]6[CH2:59][CH2:58]6)[CH2:62][CH2:63]5)=[O:27])=[CH:24][C:23]=4[O:31][CH3:32])=[N:20][C:7]2=3)[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

4

Reactant 3

HCID 9658751-(Cyclopropylmethyl)piperazineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 252529054-(9-Cyclopentyl-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

Product 1

HCID 57955515HCID 57955515, compound

Procedure

The title compound was synthesized from 4-(9-Cyclopentyl-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 1-(cyclopropylmethyl)piperazine. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.07 (br. s., 2H) 0.47 (br. s., 2H) 1.55 (br. s., 5H) 1.68 (br. s., 2H) 1.90 (br. s., 2H) 2.21 (br. s., 1H) 2.40-2.48 (m, 3H) 3.31 (s, 4H) 3.32 (br. s., 3H) 3.88 (s, 3H) 4.03 (t, J=13.89 Hz, 2H) 4.64-4.76 (m, 1H) 6.96 (d, J=8.84 Hz, 1H) 7.04 (s, 1H) 8.00 (s, 1H) 8.15 (d, J=7.83 Hz, 1H) 8.23 (s, 1H). [M+H] calculated for C29H37F2N7O3, 570. found 570.

Workup

  1. customas described in the general procedure for amide bond synthesis

Sources & evidence

ORD record
ord-dbd65c8cd1c24915ae3f91db5d037a96
Source dataset
uspto-grants-2011_09
Patent number
US08026234B2

Reaction notes

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