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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → 2-[(Cyclopropylmethyl-amino)-methyl]-3,5,7,8-tetrahydro-pyrano[4,3-d]pyrimidin-4-one

HRID 713395
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HRID 713395 반응식
[CH:1]1([CH2:4][N:5]([CH2:13][C:14]2[NH:15][C:16](=[O:24])[C:17]3[CH2:23][O:22][CH2:21][CH2:20][C:18]=3[N:19]=2)C(=O)OC(C)(C)C)[CH2:3][CH2:2]1.C(OCC)C>Cl.O1CCOCC1>[CH:1]1([CH2:4][NH:5][CH2:13][C:14]2[NH:15][C:16](=[O:24])[C:17]3[CH2:23][O:22][CH2:21][CH2:20][C:18]=3[N:19]=2)[CH2:3][CH2:2]1
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참가 물질

5

반응물 2

HCID 3283Diethyl EtherHCID 136627243tert-Butyl N-(cyclopropylmethyl)-N-[(4-oxo-4,5,7,8-tetrahydro-3H-pyrano[4,3-d]pyrimidin-2-yl)methyl]carbamate

생성물 1

HCID 1362440742-[(Cyclopropylmethyl-amino)-methyl]-3,5,7,8-tetrahydro-pyrano[4,3-d]pyrimidin-4-one수율 121.8%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane
용매

실험 절차

tert-butyl cyclopropylmethyl((4-oxo-4,5,7,8-tetrahydro-3H-pyrano[4,3-d]pyrimidin-2-yl)methyl)carbamate (5.639 g, 16.81 mmol) was dissolved in 4 N HCl in dioxane (40 mL) and stirred at room temperature after approximately 5 min a white suspension formed and the reaction was allowed to stir overnight. 100 mL diethyl ether was added and the reaction mixture was filtered, washed with diethyl ether (2×25 mL) and dried in vacuo to yield the title compound as a white solid (4.819 g).

후처리

  1. customformed
  2. stirringto stir overnight
  3. filtrationthe reaction mixture was filtered
  4. washwashed with diethyl ether (2×25 mL)
  5. customdried in vacuo

출처 및 근거

ORD 기록
ord-abd6badb1f7041fd95650acc9883a40e
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181266B2

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