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HRID 10974作成日:2026年10月26日

Allyl iodide → 6-allyl-3-benzyloxycarbonylamino-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/10974

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl iodideHCID 11166—
反応物tert-Butyl (S)-3-{[(benzyloxy)carbonyl]amino}-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylateHCID 54224046—
反応物3-benzyloxycarbonylamino-6-methyl-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic Acid tert-butyl EsterHCID 69600879—
生成物6-allyl-3-benzyloxycarbonylamino-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic Acid tert-butyl EsterHCID 6960095055%

反応手順

According to the procedure for the preparation of intermediate 19a, alkylation of intermediate 1g (250 mg, 0.649 mmol) with allyl iodide afforded 153 mg (55%) of intermediate 20a. MS (ESI) 426.4 (M+H+), 448.4 (M+Na+).

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-7977f68c4da0489ebc38176d5555ba59
出典メモuspto-grants-2006_08