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Dicyclohexylcarbodiimide → Acetic acid N-hydroxysuccinimide ester

HRID 2394237
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HRID 2394237 반응식
CN1C(S[CH2:8][C:9]([OH:11])=[O:10])=NN=N1.O[N:13]1[C:17](=[O:18])[CH2:16][CH2:15][C:14]1=[O:19].C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[O:19]=[C:14]1[CH2:15][CH2:16][C:17](=[O:18])[N:13]1[O:11][C:9](=[O:10])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10868DicyclohexylcarbodiimideHCID 80170N-HydroxysuccinimideHCID 3155947[(1-methyl-1h-tetrazol-5-yl)thio]acetic acid

생성물 1

HCID 84460Acetic acid N-hydroxysuccinimide ester

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5.2 g (885 mmol) (1-methyl-1H-tetrazol-5-ylsulfanyl)-acetic acid (CAS Reg. No 55862-52-7; Saito, Seiki et al, Synlett (1993), 2, 139-40 ; 29) were dissolved in 100 ml dimetylformamide. Then 3.44 g (32.84 mmol) N-hydroxysuccinimide were added. Then 6.78 g N,N'-dicyclohexylcarbodiimid were added. After a few minutes white crystals were obtained. The suspension was stirred for further five days. The crystals were filtered off. Dimethylformamide was removed in vacuum. The residue was taken up in 60 ml ethyl acetate at 60° C., filtered off, washed with 30 ml ethylacetate (three times) and dried at high vacuum. 1-Methyl-1H-tetrazol-5-ylsulfanyl)-acetic acid 2,5-dioxo-pyrrolidin-1-yl ester was obtained.

후처리

  1. customAfter a few minutes white crystals were obtained
  2. filtrationThe crystals were filtered off
  3. customDimethylformamide was removed in vacuum
  4. customwas taken up in 60 ml ethyl acetate at 60° C.
  5. filtrationfiltered off
  6. washwashed with 30 ml ethylacetate (three times)
  7. customdried at high vacuum

출처 및 근거

ORD 기록
ord-1783160472344e6f93b5a7ecf9e68367
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05811419

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