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Sodium Bicarbonate → S-Ethyl O-(N3,N7,N12,N16-tetra(t-butoxycarbonyl)-3,7,12,16-tetraazahexadecanoyl oxy)methyl carbonothioate

HRID 1397113
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HRID 1397113 반응식
[C:1](=[O:8])([O:5][CH2:6]I)[S:2][CH2:3][CH3:4].[C:9]([O:13][C:14]([N:16]([CH2:21][CH2:22][CH2:23][N:24]([C:48]([O:50][C:51]([CH3:54])([CH3:53])[CH3:52])=[O:49])[CH2:25][CH2:26][CH2:27][CH2:28][N:29]([C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[CH2:30][CH2:31][CH2:32][NH:33][C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH2:17][C:18]([OH:20])=[O:19])=[O:15])([CH3:12])([CH3:11])[CH3:10].C([O-])(O)=O.[Na+]>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.C(Cl)Cl.O.C(Cl)Cl>[C:1](=[O:8])([O:5][CH2:6][O:20][C:18](=[O:19])[CH2:17][N:16]([C:14]([O:13][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:15])[CH2:21][CH2:22][CH2:23][N:24]([C:48]([O:50][C:51]([CH3:54])([CH3:53])[CH3:52])=[O:49])[CH2:25][CH2:26][CH2:27][CH2:28][N:29]([C:41]([O:43][C:44]([CH3:45])([CH3:46])[CH3:47])=[O:42])[CH2:30][CH2:31][CH2:32][NH:33][C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[S:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 516892Sodium BicarbonateHCID 11006845N3,N7,N12,N16-Tetra(t-butoxycarbonyl)-3,7,12,16-tetraazahexadecanoic acidHCID 11436522(Ethylsulfanyl)(iodomethoxy)methanone

생성물 1

HCID 86666527S-Ethyl O-(N3,N7,N12,N16-tetra(t-butoxycarbonyl)-3,7,12,16-tetraazahexadecanoyl oxy)methyl carbonothioate수율 92.3%

시약·촉매·용매 3

HCID 94433
Tetrabutylammonium hydrogen sulfate
촉매
HCID 6344Dichloromethane용매
HCID 21908982Water methylene chloride용매

실험 절차

S-Ethyl O-iodomethyl carbonothioate (423 mg, 1.72 mmol) was added to a stirring mixture of 31 (1.13 g, 1.71 mmol), NaHCO3 (298 mg, 3.55 mmol) and tetrabutylammonium hydrogensulfate (588 mg, 1.73 mmol) in CH2Cl2/H2O (1:1, 17 mL) and the resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with CH2Cl2 (80 mL) and the aqueous layer was discarded. The organic layer was washed with saturated aqueous NH4Cl, saturated aqueous NaCl, dried over Na2SO4 then concentrated under reduced pressure. The residue was resuspended in Et2O, filtered and again concentrated under reduced pressure. The crude material was purified by silica gel chromatography (25%-60% EtOAc in hexanes over 10 column volumes) to give the colourless liquid 32 (1.23 g, 92%): 1H NMR (400 MHz, CDCl3): δ 1.32 (t, J=7.3, 3H), 1.41-1.47 (m, 40H), 1.61-1.75 (m, 4H), 2.89 (q, J=7.3, 2H), 3.10-3.31 (m, 12H), 3.92 (s, 4/7 of 2H, rotamer A), 4.01 (s, 3/7 of 2H, rotomer B), 5.84 (s, 2H).

후처리

  1. washThe organic layer was washed with saturated aqueous NH4Cl, saturated aqueous NaCl
  2. dry with materialdried over Na2SO4
  3. concentrationthen concentrated under reduced pressure
  4. filtrationfiltered
  5. concentrationagain concentrated under reduced pressure
  6. customThe crude material was purified by silica gel chromatography (25%-60% EtOAc in hexanes over 10 column volumes)

출처 및 근거

ORD 기록
ord-ef97f8d2e01b45db82fa8cc2c8a27706
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901072B2

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