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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2222972생성일: 2026년 10월 25일

Formaldehyde → Methyl 1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/2222972

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium AcetateHCID 517045—
반응물2-[(S)-2-[(R)-4-(4-methoxy-phenyl)-2,5-dioxo-imidazolidin-1-yl]-3-(4-nitro-phenyl)-propionylamino]-thiazole-4-carboxylic acid methyl esterHCID 58615496—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물Methyl 1,3-thiazole-4-carboxylateHCID 277341483.8%

반응 단계

To a solution of 2-[(S)-2-[(R)-4-(4-methoxy-phenyl)-2,5-dioxo-imidazolidin-1-yl]-3-(4-nitro-phenyl)-propionylamino]-thiazole-4-carboxylic acid methyl ester (53.9 mg, 0.1 mmol) in tetrahydrofuran (10 mL) was added sodium acetate (60 mg, 0.44 mmol), 37% w/w aqueous formaldehyde solution (0.033 mL, 0.44 mmol) and 10% palladium on carbon (30 mg) and the mixture shaken under an atmosphere of hydrogen at 50 psi pressure in a Parr apparatus for 72 hours. The reaction mixture was filtered through a pad of Celite® and washed through with additional tetrahydrofuran. The filtrate was concentrated in vacuo, the residue was dissolved in dichloromethane, washed with water, saturated aqueous sodium bicarbonate, dried with sodium sulfate and concentrated in vacuo to give the crude product as a yellow solid. Purification by reverse phase HPLC using a C18 stationary phase gradient eluted from 10% up to 90% acetonitrile in water gave 2-(S)-3-(4-dimethylamino-phenyl)-2-[(R)-4-(4-methoxy-phenyl)-2,5-dioxo-imidazolidin-1-yl]-propionylamino}-thiazole-4-carboxylic acid methyl ester as a colorless solid (12 mg, 22%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07371869B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-5e96646c3cd64def9d1f73300964f5b4
출처 메모uspto-grants-2008_05