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Hydrochloric Acid → (R)-(R)-quinuclidin-3-yl 2-amino-2-phenylacetate bis hydrochloride

HRID 2279936
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인쇄 미리보기

반응식

HRID 2279936 반응식
[N:1]12[CH2:8][CH2:7][CH:4]([CH2:5][CH2:6]1)[C@@H:3]([O:9][C:10](=[O:26])[C@H:11]([NH:18]C(OC(C)(C)C)=O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:2]2.[ClH:27].CCOCC>O1CCOCC1>[ClH:27].[ClH:27].[NH2:18][C@H:11]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:10]([O:9][C@@H:3]1[CH:4]2[CH2:5][CH2:6][N:1]([CH2:8][CH2:7]2)[CH2:2]1)=[O:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 67607970(R)-((R)-quinuclidin-3-yl) 2-(tert-butoxycarbonylamino)-2-phenylacetate

생성물 1

HCID 86720688(R)-(R)-quinuclidin-3-yl 2-amino-2-phenylacetate bis hydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of (R)—(R)-quinuclidin-3-yl2-((tert-butoxycarbonyl)amino)-2-phenylacetate I-46 (0.608 g, 1.687 mmol) in anhydrous dioxane (6 mL) was added with 2M HCl in ether (5.2 mL, 10.4 mmol). The reaction mixture was stirred at room temperature for 20 h. The solvent was removed in vacuo to afford the title compound as a white solid (0.564 g, quantitative yield).

후처리

  1. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-e84d8bcb586a481faf81e15354d7d8df
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133185B2

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