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HRID 10976作成日:2026年10月25日

6-allyl-3-benzyloxycarbonylamino-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic Acid → benzyl N-[6-[[4-[N-[(2-methylpropan-2-yl)oxycarbonyl]carbamimidoyl]phenyl]methylcarbamoyl]-4-oxo-6-prop-2-enyl-7,8-dihydropyrrolo[1,2-a]pyrimidin-3-yl]carbamate

https://huagongshe.com/reaction/10976

反応式

関与物質

役割名称HCID仕込み量
反応物6-allyl-3-benzyloxycarbonylamino-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic AcidHCID 21979697—
反応物tert-butyl N-[4-(aminomethyl)benzenecarboximidoyl]carbamateHCID 145832046—
生成物benzyl N-[6-[[4-[N-[(2-methylpropan-2-yl)oxycarbonyl]carbamimidoyl]phenyl]methylcarbamoyl]-4-oxo-6-prop-2-enyl-7,8-dihydropyrrolo[1,2-a]pyrimidin-3-yl]carbamateHCID 14585720386%

反応手順

According to the procedure for the preparation of intermediate 19c, intermediate 20b (50 mg, 0.135 mmol) was coupled with [(4-aminomethyl-phenyl)-imino-methyl]-carbamic acid tert-butyl ester to afford 70 mg (86%) of intermediate 20c.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094783B2
出典データセットuspto-grants-2006_08
ORD IDord-1f57f987a2284ab48972c433a6c34bef
出典メモuspto-grants-2006_08