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Sodium Bicarbonate → HCID 67236011, 화합물

HRID 447163
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HRID 447163 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[S:15][C:16]3[CH:22]=[C:21]([C:23](OCC)=[O:24])[CH:20]=[CH:19][C:17]=3[N:18]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[BH4-].[Li+].C(=O)(O)[O-].[Na+]>C1COCC1>[OH:24][CH2:23][C:21]1[CH:20]=[CH:19][C:17]2[N:18]=[C:14]([N:11]3[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:2])([CH3:4])[CH3:3])=[O:7])[CH2:9][CH2:10]3)[S:15][C:16]=2[CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 4148881Lithium borohydrideHCID 67236140Ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)benzo[d]thiazole-6-carboxylate

생성물 1

HCID 67236011HCID 67236011, 화합물수율 101.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)benzo[d]thiazole-6-carboxylate (1.1 g) was dissolved in dry THF (50 mL) and lithium borohydride (67 mg) was added. The resulting mixture was stirred overnight at room temperature, then heated to reflux for 24 hours. Saturated aqueous sodium bicarbonate was added and the resulting mixture was extracted with ethyl acetate. The resulting solution was concentrated to yield tert-butyl 4-(6-(hydroxymethyl)benzo[d]thiazol-2-yl)piperazine-1-carboxylate as a white solid (1.0 g). MS: 350.3 (M+H).

후처리

  1. temperatureheated
  2. temperatureto reflux for 24 hours
  3. extractionthe resulting mixture was extracted with ethyl acetate
  4. concentrationThe resulting solution was concentrated

출처 및 근거

ORD 기록
ord-6631130a907c4973a12d54452a0e314d
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481547B2

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