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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 912323Erstellt: 26. Oktober 2026

Thiophosgene → 4-(2-Amino-pyrimidin-5-yl)-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carbothioic acid [4-(4-ethyl-piperazine-1-carbonyl)-phenyl]-amide

https://huagongshe.com/reaction/912323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiophosgeneHCID 10040—
Edukt(4-Aminophenyl)(4-ethylpiperazin-1-yl)methanoneHCID 1132820—
EduktBis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amineHCID 45258862—
Edukt4-(4-Ethyl-piperazin-1-yl)-2,6-difluoro-phenylamineHCID 59244379—
Produkt4-(2-Amino-pyrimidin-5-yl)-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carbothioic acid [4-(4-ethyl-piperazine-1-carbonyl)-phenyl]-amideHCID 5924460262%

Reaktionsschritte

Using bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine (80.9 mg) and (4-amino-phenyl)-(4-ethyl-piperazin-1-yl)-methanone (42 mg) obtained in Step B in Example 1-D-103 instead of 4-(4-ethyl-piperazin-1-yl)-2,6-difluoro-phenylamine, and thiophosgene (22.9 μl) instead of triphosgene, in the same manner as Step D in Example 1-D-18, 4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carbothioic acid [4-(4-ethyl-piperazine-1-carbonyl)-phenyl]-amide was obtained as a crude product. The PMB groups were removed according to Deprotection method 3, to obtain the desired compound (D-232) as a colorless solid (54.1 mg, 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08022205B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-161f2457ed2543a78674548ea4f62550
Quellennotizuspto-grants-2011_09