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Hydrochloric Acid → Tert-butyl (1-(2-(1,2-dihydroxyethyl)quinolin-8-yl)piperidin-4-yl)methylcarbamate

HRID 339672
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HRID 339672 반응식
[C:1]([O:5][C:6](=[O:32])[NH:7][CH2:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:16]=[CH:17][CH:18]=[C:19]3[C:24]=2[N:23]=[C:22]([CH:25]2[CH2:29][O:28]C(C)(C)[O:26]2)[CH:21]=[CH:20]3)[CH2:11][CH2:10]1)([CH3:4])([CH3:3])[CH3:2].Cl>C1COCC1.CCOC(C)=O.C([O-])(O)=O.[Na+]>[C:1]([O:5][C:6](=[O:32])[NH:7][CH2:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:16]=[CH:17][CH:18]=[C:19]3[C:24]=2[N:23]=[C:22]([CH:25]([OH:26])[CH2:29][OH:28])[CH:21]=[CH:20]3)[CH2:11][CH2:10]1)([CH3:4])([CH3:2])[CH3:3]
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참가 물질

6

반응물 2

HCID 313Hydrochloric AcidHCID 86654343Tert-butyl (1-(2-(2,2-dimethyl-1,3-dioxolan-4-yl)quinolin-8-yl)piperidin-4-yl)methylcarbamate

생성물 1

HCID 86654344Tert-butyl (1-(2-(1,2-dihydroxyethyl)quinolin-8-yl)piperidin-4-yl)methylcarbamate

시약·촉매·용매 3

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매
HCID 516892
Sodium Bicarbonate
용매

실험 절차

To tert-butyl(1-(2-(2,2-dimethyl-1,3-dioxolan-4-yl)quinolin-8-yl)piperidin-4-yl)methylcarbamate (81 mg, 0.18 mmol) in THF (3 mL) was added HCl (20 mg, 0.55 mmol) (6M). The reaction was stirred for 3 hours at ambient temperature and then diluted with EtOAc (10 mL) and saturated NaHCO3 (5 mL). The phases were separated, and the organic layer was dried and concentrated to give crude product.

후처리

  1. customThe phases were separated
  2. customthe organic layer was dried
  3. concentrationconcentrated
  4. customto give crude product

출처 및 근거

ORD 기록
ord-7e6a234823d748cb8e0377c59d8a1187
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895550B2

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