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HRID 10985作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/10985

反応式

関与物質

役割名称HCID仕込み量
反応物3-benzyloxycarbonylamino-6-methoxymethyl-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic AcidHCID 21979643—
反応物tert-butyl N-[4-(aminomethyl)benzenecarboximidoyl]carbamateHCID 145832046—
生成物benzyl N-[6-(methoxymethyl)-6-[[4-[N-[(2-methylpropan-2-yl)oxycarbonyl]carbamimidoyl]phenyl]methylcarbamoyl]-4-oxo-7,8-dihydropyrrolo[1,2-a]pyrimidin-3-yl]carbamateHCID 145857230100%

反応手順

According to the procedure for the preparation of intermediate 19c, intermediate 23b (57.8 mg, 0.155 mmol) was coupled with [(4-aminomethyl-phenyl)-imino-methyl]-carbamic acid tert-butyl ester to afford 94 mg (100%) of intermediate 23c.

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-e044293813a0477f8e6f434a4d06c847
出典メモuspto-grants-2006_08