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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1880854Erstellt: 25. Oktober 2026

4-Amino-1-methylpiperidine → 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-(1-methyl-piperidin-4-yl)-3-trifluoromethyl-benzamide

https://huagongshe.com/reaction/1880854

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Amino-1-methylpiperidineHCID 2737531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-3-(trifluoromethyl)benzoic acidHCID 58015002—
Produkt4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-(1-methyl-piperidin-4-yl)-3-trifluoromethyl-benzamideHCID 25253678—

Reaktionsschritte

The title compound was synthesized from 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-3-(trifluoromethyl)benzoic acid as described in the General procedure for amide bond synthesis using HATU and 1-methylpiperidin-4-amine. The final compound was purified by reverse phase HPLC and basified to give the free base. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.34-1.67 (m, 9 H) 1.70-1.85 (m, 3 H) 2.13 (br. s., 1 H) 2.27 (s, 3 H) 2.84-2.93 (m, 1 H) 3.32 (s, 3 H) 3.74-3.86 (m, 1 H) 4.00 (t, J=14.0 Hz, 1 H) 4.50 (quin, 1 H) 7.96 (d, J=8.6 Hz, 1 H) 8.12 (dd, 1 H) 8.20 (s, 1 H) 8.21 (s, 1 H) 8.48 (d, J=7.8 Hz, 1 H) 8.52 (s, 1 H). [M+H] calc'd for C27H32F5N7O2, 582; found 582.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08318727B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-32509140e43b46ba9e6decc6a3796d9f
Quellennotizuspto-grants-2012_11