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Hexylamine → HCID 86599750, 화합물

HRID 1393917
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HRID 1393917 반응식
[CH2:1]([O:8][C:9]([NH:11][C@H:12]1[CH2:17][CH2:16][CH2:15][NH:14][C:13]1=[O:18])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[P:19](Cl)(Cl)(Cl)=[O:20].[CH2:24]([NH2:30])[CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>O1CCCC1>[CH2:1]([O:8][C:9]([NH:11][C@H:12]1[CH2:17][CH2:16][CH2:15][N:14]([P:19]([NH:30][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])([NH:30][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[O:20])[C:13]1=[O: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

5

반응물 3

HCID 8102HexylamineHCID 24813Phosphorus oxychlorideHCID 11482034Benzyl [(3S)-2-oxopiperidin-3-yl]carbamate

생성물 1

HCID 86599750HCID 86599750, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of (3S)-3-benzyloxycarbonylamino-2-piperidone (2.48 g, 9.99 mmol) in tetrahydrofuran (25 mL) was cooled at an external temperature of −78° C., followed by adding dropwise thereto an n-butyllithium-hexane solution (1.54 M, 6.2 mL, 9.548 mmol) over a period of 10 minutes, and the resulting mixture was stirred at the same temperature for 1.5 hours. Subsequently, a solution of phosphorus oxychloride (1.53 g, 9.98 mmol) in tetrahydrofuran (5 mL) was added thereto and stirred for 1.25 hours, after which n-hexylamine (d=0.76, 6.0 mL, 45.06 mmol) was added thereto and the resulting mixture was stirred at room temperature for 10 minutes.

후처리

  1. additionby adding dropwise
  2. stirringstirred for 1.25 hours
  3. stirringthe resulting mixture was stirred at room temperature for 10 minutes

출처 및 근거

ORD 기록
ord-db3f9d202367461b8ec6121a666081fd
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07348318B2

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