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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171786생성일: 2026년 10월 27일

Triethylamine → 1-[(5-Chloro-1H-indol-2-yl)methyl]-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-one

https://huagongshe.com/reaction/1171786

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzoyl isothiocyanateHCID 68284—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물5-Chloro-1H-indole-2-carbaldehydeHCID 12203318—
반응물3-Amino-2-ethoxycarbonylpyrrole hydrochlorideHCID 16427091—
촉매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물1-[(5-Chloro-1H-indol-2-yl)methyl]-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-oneHCID 1153003230.2%

반응 단계

5-Chloro-1H-indole-2-carbaldehyde (0.15 g, 0.76 mmol), NaCNBH3 (0.040 g, 0.63 mmol) and Et3N (0.088 mL, 0.63 mmol) was added to a stirred solution of 3-amino-1H-pyrrole-2-carboxylic acid ethyl ester hydrochloride (0.12 g, 0.63 mmol) in methanol (3 mL). The resulting mixture was stirred at r.t. overnight. The reaction mixture was heated to 50° C. Additional NaCNBH3 (0.5 equiv.) was added and the mixture was stirred at 50° C. for 3 h. A few drops of HOAc was added, and after 1 h the reaction mixture was cooled to r.t. and was concentrated in vacuo. The residue was dissolved in CH2Cl2 (2 mL) and methanol (2 mL). Benzoyl isothiocyanate (0.093 mL, 0.69 mmol) was added and after stirring at r.t. for 1 h the mixture was concentrated in vacuo. The residue was dissolved in ammonia (7N in methanol, 3 mL) and heated at 80° C. for 2 h. The precipitated product was filtered and washed through with methanol and diethyl ether, followed by purification by preparative HPLC, obtaining 0.063 g (30%) of the title compound as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829707B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-26b1f232fbfc403e9270eed96811877f
출처 메모uspto-grants-2010_11