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1-(t-Butoxycarbonyl)4-((2-benzyl)tetrazol-5-yl)piperidine → 4-((2-Benzyl)tetrazol-5-yl)piperidine

HRID 1068179
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인쇄 미리보기

반응식

HRID 1068179 반응식
[C:1]([O:5]C([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[N:15]=[N:16][N:17]([CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[N:18]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[CH2:26]([Cl:28])[Cl:27].C(O)(C(F)(F)F)=[O:30]>>[CH2:26]([Cl:28])[Cl:27].[CH3:1][OH:5].[NH4+:8].[OH-:30].[CH2:19]([N:17]1[N:16]=[N:15][C:14]([CH:11]2[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]2)=[N:18]1)[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 181875061-(t-Butoxycarbonyl)4-((2-benzyl)tetrazol-5-yl)piperidineHCID 21863450Trifluoroacetic acid methylene chloride

생성물 2

HCID 181874764-((2-Benzyl)tetrazol-5-yl)piperidine수율 94%HCID 21896990Dichloromethane methanol ammonium hydroxide

실험 절차

A solution of 85 mg (0.25 mmol) of 1-(t-butoxycarbonyl)-4-((2-benzyl)tetrazol-5-yl)piperidine (from Step C) in 2 mL of 1:1 v/v CH2Cl2/TFA was stirred at rt for 2 h. The solution was concentrated. Flash chromatography on silica gel using 19:1:0.1 v/v/v CH2Cl2/MeOH/NH4OH as the eluant afforded 57 mg (94%) of the title compound.

후처리

  1. concentrationThe solution was concentrated

출처 및 근거

ORD 기록
ord-f101cb2766d24b38978938d4fe044869
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06248755B1

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