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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242316생성일: 2026년 10월 27일

Potassium Carbonate → 1-Pyrrolidinecarboxylic acid, 3-[[5,6,7,8-tetrahydro-6-(phenylmethyl)pyrido[4,3-d]pyrimidin-4-yl]amino]-, 1,1-dimethylethyl ester, (3S)-

https://huagongshe.com/reaction/242316

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물tert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
반응물6-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido(4,3-d)pyrimidineHCID 25324046—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물1-Pyrrolidinecarboxylic acid, 3-[[5,6,7,8-tetrahydro-6-(phenylmethyl)pyrido[4,3-d]pyrimidin-4-yl]amino]-, 1,1-dimethylethyl ester, (3S)-HCID 5749532397%

반응 조건

온도120 °C

반응 단계

(S)-tert-Butyl-3-aminopyrrolidine-1-carboxylate (50 g, 192.5 mmol) was added to 6-benzyl-4-chloro-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine (39.440 g, 211.8 mmol) in NMP (200 mL) solution followed by the addition of K2CO3 (39.9 g, 288.8 mmol). The mixture was heated to 120° C. for 20 h. The mixture was allowed to cool, partitioned between water (300 mL) and ethylacetate (500 mL). the bottom aqueous phase was discarded and the upper organic phase was washed with brine (150 mL) and concentrated in vacuo to provide crude (S)-3-(6-benzyl-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester as a pale yellow foam (76.44 g, 97% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653092B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-c02289d97acb40bd9157b437a574d352
출처 메모uspto-grants-2014_02