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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-butyl N-(2-{[(benzyloxy)carbonyl]amino}ethyl)-3-methyl-L-valinate → HCID 67405688, 화합물

HRID 1174404
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인쇄 미리보기

반응식

HRID 1174404 반응식
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][NH:14][C@H:15]([C:20]([O:22]C(C)(C)C)=[O:21])[C:16]([CH3:19])([CH3:18])[CH3:17])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>Cl.O1CCOCC1>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][NH:14][C@H:15]([C:20]([OH:22])=[O:21])[C:16]([CH3:19])([CH3:17])[CH3:18])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67407977tert-butyl N-(2-{[(benzyloxy)carbonyl]amino}ethyl)-3-methyl-L-valinate

생성물 1

HCID 67405688HCID 67405688, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

The product from Example 180A (0.870 mmol) was dissolved in an HCl solution in dioxane (5.0 mL, 4 N), and the mixture was stirred at room temperature for 12 hours. The solvent was evaporated to afford the title compound as the hydrochloride salt. The residue was used without further purification.

후처리

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
The solvent was evaporated

출처 및 근거

ORD 기록
ord-a7b90aa7d1a0457587b3c65ab332ad53
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07834043B2

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