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Phosgene → 8-chlorodibenz[b,f][1,4]thiazepine-10(11H)-carbonyl chloride

HRID 1756556
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반응식

HRID 1756556 반응식
[C:1]([Cl:4])(Cl)=[O:2].[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[C:10]([NH2:12])[CH:11]=1.[CH2:20](N(CC)CC)C>O1CCCC1>[Cl:5][C:6]1[CH:7]=[CH:8][C:9]2[S:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[CH2:20][N:12]([C:1]([Cl:4])=[O:2])[C:10]=2[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6371PhosgeneHCID 8471TriethylamineHCID 20637175-Chloro-2-phenylsulfanyl-phenylamine

생성물 1

HCID 229217168-chlorodibenz[b,f][1,4]thiazepine-10(11H)-carbonyl chloride

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a cold (ice-H2O bath), stirred solution of phosgene (1.93M in toluene; 8.6 mL) in anhydrous tetrahydrofuran (40 mL) under a nitrogen atmosphere is added, dropwise, a solution of the title product of Example 48 (2.00 g) and triethylamine (1.3 mL) in anhydrous tetrahydrofuran (30 mL). The resulting mixture is stirred at room temperature for 90 minutes, and the solvent is then evaporated in vacuo to provide the title product.

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후처리

  1. additionis added
  2. customthe solvent is then evaporated in vacuo

출처 및 근거

ORD 기록
ord-5dbe819bb5524b6c81c1c9ebe4c636d6
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05441950

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