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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2214538생성일: 2026년 10월 26일

Formaldehyde → methyl 4-[[3-[(3,4-dichlorophenyl)methyl-methyl-carbamoyl]-4-hydroxy-5-oxo-2H-pyrrol-1-yl]methyl]benzoate

https://huagongshe.com/reaction/2214538

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물TriethylamineHCID 8471—
반응물Benzoic acid, 4-(aminomethyl)-, hydrochloride (1:1)HCID 105553—
반응물3-[3-[3-[(3,4-dichlorophenyl)methyl-methyl-carbamoyl]-4-hydroxy-5-oxo-2H-pyrrol-1-yl]propanoylamino]propanoic acidHCID 54691726—
반응물N-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamideHCID 69655735—
생성물methyl 4-[[3-[(3,4-dichlorophenyl)methyl-methyl-carbamoyl]-4-hydroxy-5-oxo-2H-pyrrol-1-yl]methyl]benzoateHCID 5469821026%

반응 단계

N-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamide (Compound 37-A) was treated with paraformaldehyde and 4-(aminomethyl)-benzoate hydrochloride salt with 1 equivalent of triethyl amine as described in the preparation of Compound 37. The title compound was purified by chromatography (YMC Combiprep ODS-A, 30 mm×50 mm, MeOH/H2O/0.1% TFA) to yield the title compound as a yellow foam (0.060 g, 26% yield). 1H NMR (300 MHz, CDCl3) δ: 2.98 (s, 3H), 3.91 (s, 3H), 4.05 (s, 2H), 4.56 (s, 2H), 7.07 (dd, J=1.8 Hz, J=8.1 Hz, 1H), 7.30 (m, 3H), 7.40 (m, 1H), 8.00 (d, J=8.1 Hz, 1H). HRMS (M−H) calcd for C22H20N2Cl2O5: 461.0671. found: 461.0690.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07109186B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-79a6817598264c5b9748061ea0849020
출처 메모uspto-grants-2006_09