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Hydrochloric Acid → HCID 67366603, 화합물

HRID 81342
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HRID 81342 반응식
[ClH:1].C(OC(=O)[NH:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C:19](=[NH:21])[NH2:20])=[CH:15][CH:14]=1)(C)(C)C.C(Cl)[Cl:24].CO>CO>[ClH:24].[ClH:1].[NH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]([NH2:21])=[NH:20])=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 21226129Dichloromethane methanolHCID 67366022[4-(4-Carbamimidoylphenyl)butyl]carbamic acid tert-butyl ester

생성물 1

HCID 67366603HCID 67366603, 화합물수율 94%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

12 N hydrochloric acid (0.71 mL, 8.6 mmol) was added dropwise into a stirring solution of [4-(4-carbamimidoylphenyl)butyl]carbamic acid tert-butyl ester (59) (124 mg, 0.43 mmol) in methanol (2 mL). After stirring for 2.5 h, TLC (methylene chloride/methanol/concentrated ammonium hydroxide, 6:3:1) indicated reaction completion. The reaction mixture was vacuum filtered. The solvent was removed from the filtrate by evaporation. Residual water was further removed as an azeotrope of toluene/methanol (1:1). Placement of the residue under vacuum for 2 h afforded the product 60 (106 mg, 94%) as a yellow foamy solid. 1H NMR (300 MHz, DMSO-d6) δ 1.62 (m, 4H), 2.70 (t, 2H), 2.78 (m, 2H), 3.49 (br s, 1H), 7.47 (d, 2H), 7.82 (d, 2H), 8.13 (br s, 3H), 9.25 (s, 2H), 9.42 (s, 2H).

후처리

  1. customreaction completion
  2. filtrationfiltered
  3. customThe solvent was removed from the filtrate by evaporation
  4. customResidual water was further removed as an azeotrope of toluene/methanol (1:1)

출처 및 근거

ORD 기록
ord-d54b1b13349a4e9aa1f8bf02f58fb92d
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846688B2

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