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4-Methylmorpholine → (1S)-[1-Hydroxymethyl-3-(tritylcarbamoyl)propyl]carbamic Acid Benzyl Ester

HRID 1057748
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HRID 1057748 반응식
CN1CCOCC1.ClC(OCC)=O.[NH:14]([C:43]([O:45][CH2:46][C:47]1[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=1)=[O:44])[C@H:15]([C:40](O)=[O:41])[CH2:16][CH2:17][C:18](=[O:39])[NH:19][C:20]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[BH4-].[Na+]>C1COCC1.O>[CH2:46]([O:45][C:43](=[O:44])[NH:14][C@H:15]([CH2:40][OH:41])[CH2:16][CH2:17][C:18](=[O:39])[NH:19][C:20]([C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1)[C:47]1[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 79724-MethylmorpholineHCID 10928Ethyl chloroformateHCID 4311764Sodium borohydrideHCID 10962399Z-Gln(Trt)-OH

생성물 1

HCID 10505827(1S)-[1-Hydroxymethyl-3-(tritylcarbamoyl)propyl]carbamic Acid Benzyl Ester

시약·촉매·용매 2

HCID 962Water
용매
HCID 8028Tetrahydrofuran용매

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온도
23 °C

실험 절차

4-Methylmorpholine (1.89 mL, 17.2 mmol, 1 equiv) and ethyl chloroformate (1.65 mL, 17.3 mmol, 1 equiv) were added to a mixture of commercially available Cbz-Gln(Trt)-OH (9.00 g, 17.2 mmol, 1 equiv) in THF (23 mL) at −10° C. After stirring 20 min, the reaction mixture was filtered and the filtrate was added dropwise to a suspension of NaBH4 (1.47 g, 38.9 mmol, 2.25 equiv) in H2O (10 mL) at 0° C. The resulting mixture was allowed to warm to 23° C. and stirred for 5 h. It was then cooled again to 0° C., quenched by the careful addition of 1 N HCl (30 mL) and then partitioned between MTBE (500 mL) and brine (2×100 mL). The organic phase was dried over Na2SO4 and evaporated to provide the title intermediate which was used without further purification.

후처리

  1. filtrationthe reaction mixture was filtered
  2. stirringstirred for 5 h
  3. temperatureIt was then cooled again to 0° C.
  4. customquenched by the careful addition of 1 N HCl (30 mL)
  5. custompartitioned between MTBE (500 mL) and brine (2×100 mL)
  6. dry with materialThe organic phase was dried over Na2SO4
  7. customevaporated

출처 및 근거

ORD 기록
ord-922dbb5c2c104c169669214862f2bb92
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06514997B2

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