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HRID 38528作成日:2026年10月24日

3-Chloro-4-(3-fluorobenzyloxy)aniline → Ethyl 4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-5,7-dihydro-6H-pyrrolo[3',4':4,5]thieno[2,3-d]pyrimidine-6-carboxylate

https://huagongshe.com/ja/reaction/38528

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 7059263—
反応物Ethyl12-chloro-7-thia-4,9,11-triazatricyclo[6.4.0.02,6]dodeca-1(8),2(6),9,11-tetraene-4-carboxylateHCID 58116864—
生成物Ethyl 4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-5,7-dihydro-6H-pyrrolo[3',4':4,5]thieno[2,3-d]pyrimidine-6-carboxylateHCID 5811687765%

反応手順

In analogy to Example 22A, the title compound was prepared from ethyl 4-chloro-5,7-dihydro-6H-pyrrolo[3′,4′:4,5]thieno[2,3-d]pyrimidine-6-carboxylate from Example 21A (100 mg, 0.35 mmol) and 3-chloro-4-[(3-fluorobenzyl)oxy]aniline from Example 4A (93 mg, 0.37 mmol) to give 157 mg (72% purity, 65% yield), which was used in the next step without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524722B2
出典データセットuspto-grants-2013_09
ORD IDord-594468d559704b868d2e46c6f7f82eb2
出典メモuspto-grants-2013_09