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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 1-Benzhydryl-3-hydrazinylazetidine dihydrochloride

HRID 46356
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인쇄 미리보기

반응식

HRID 46356 반응식
[C:1]1([CH:7]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[N:8]2[CH2:11][CH:10]([NH:12][NH:13]C(OC(C)(C)C)=O)[CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:27]>O1CCOCC1>[ClH:27].[ClH:27].[C:21]1([CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[N:8]2[CH2:11][CH:10]([NH:12][NH2:13])[CH2:9]2)[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 59436626Tert-butyl 2-(1-benzhydrylazetidin-3-yl)hydrazinecarboxylate

생성물 1

HCID 601459041-Benzhydryl-3-hydrazinylazetidine dihydrochloride수율 85%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

To a stirred suspension of tert-butyl 2-[1-(diphenylmethyl)azetidin-3-yl]hydrazinecarboxylate (Preparation 691, 19.3 g, 54.6 mmol) in 1,4-dioxane (64 ml) was added 4M hydrogen chloride in 1,4-dioxane (290 ml) at 0° C. and stirred at room temperature for 4 hours. Then the reaction mixture was concentrated in vacuo and the residue was triturated with diethyl ether to give 15 g (85%) of the title compound as a white solid.

후처리

  1. concentrationThen the reaction mixture was concentrated in vacuo
  2. customthe residue was triturated with diethyl ether

출처 및 근거

ORD 기록
ord-ea822b62bae84ee4846b4a48c3b0c911
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541588B2

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