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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-butyl N-[(1S,4R)-4-hydroxycycloheptyl]carbamate → (1S,4R)-4-aminocycloheptan-1-ol

HRID 1631451
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HRID 1631451 반응식
[OH:1][C@@H:2]1[CH2:8][CH2:7][CH2:6][C@H:5]([NH:9]C(=O)OC(C)(C)C)[CH2:4][CH2:3]1>Cl.O1CCOCC1>[NH2:9][C@@H:5]1[CH2:6][CH2:7][CH2:8][C@H:2]([OH:1])[CH2:3][CH2:4]1
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참가 물질

4

반응물 1

HCID 69723966tert-butyl N-[(1S,4R)-4-hydroxycycloheptyl]carbamate

생성물 1

HCID 15458399(1S,4R)-4-aminocycloheptan-1-ol

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

A sample of 23B (0.070 g, 0.31 mmol) was dissolved in 2 mL of 4M HCl in dioxane and stirred 1.5 h. The reaction was concentrated under reduced pressure to afford 23C.HCl (51 mg, quantitative yield) as a white solid. This material was used without characterization in the subsequent step.

후처리

  1. concentrationThe reaction was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-48f17da55f8149b284b04473bae9b1e7
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08791257B2

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