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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48457생성일: 2026년 10월 24일

Guanidine Hydrochloride → 6-(2,4-Diamino-pyrimidin-5-ylmethyl)-1-methyl-1H-indol-4-ol

https://huagongshe.com/ko/reaction/48457

반응식

참여 물질

역할이름HCID투입량
반응물Guanidine HydrochlorideHCID 5742—
반응물3-AnilinopropionitrileHCID 14100—
반응물1-methyl-4-(2-trimethylsilanyl-ethoxymethoxy)-1H-indole-6-carbaldehydeHCID 22742876—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-[1-methyl-4-(2-trimethylsilanyl-ethoxymethoxy)-1H-indol-6-ylmethyl]-pyrimidine-2,4-diamineHCID 69922453—
용매Dimethyl SulfoxideHCID 679—
용매EthanolHCID 702—
용매tert-ButanolHCID 6386—
용매Ethyl AcetateHCID 8857—
생성물Ammonium hydroxide methanolHCID 21894508—
생성물6-(2,4-Diamino-pyrimidin-5-ylmethyl)-1-methyl-1H-indol-4-olHCID 2274289043%

반응 조건

온도70 °C

반응 단계

5-[1-Methyl-4-(2-trimethylsilanyl-ethoxymethoxy)-1H-indol-6-ylmethyl]-pyrimidine-2,4-diamine. A warm solution of potassium tert-butylate (2.68 g, 23.4 mmol) in tert-butanol (20 mL) was added to a room temperature solution of 1-methyl-4-(2-trimethylsilanyl-ethoxymethoxy)-1H-indole-6-carbaldehyde (5.95 g, 19.5 mmol) and 3-anilinopropionitrile (3.20 g, 21.4 mmol) in methyl sulfoxide (70 mL). After 2 h the solution was diluted with ethyl acetate, washed with water and brine, dried (MgSO4), and evaporated. This material was dissolved in ethanol (70 mL) and added to a suspension of guanidine hydrochloride (6.21 g, 64.4 mmol) in ethanol (210 mL), and the mixture was stirred at 70° C. for 22 h. Most of the solvent was distilled off, and the residue was partitioned between water and ether. The organic layer was washed with brine, dried (MgSO4), and evaporated. Flash chromatography (SiO2; CH2CL2/MeOH/NH4OH 19:1:0.05) afforded the title compound (3.32 g, 43%).Yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703397B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-aa6521f3357140e79c9ec53c35307513
출처 메모uspto-grants-2004_03