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Cyanogen Bromide → HCID 178422405, 화합물

HRID 717207
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HRID 717207 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([B:8]2[O:12][C:11]([CH3:14])([CH3:13])[C:10]([CH3:16])([CH3:15])[O:9]2)[CH:5]=[C:4]([NH2:17])[C:3]=1[NH2:18].[N:19]#[C:20]Br>CO>[CH3:1][C:2]1[C:3]2[NH:18][C:20]([NH2:19])=[N:17][C:4]=2[CH:5]=[C:6]([B:8]2[O:12][C:11]([CH3:14])([CH3:13])[C:10]([CH3:16])([CH3:15])[O:9]2)[CH:7]=1
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참가 물질

4

반응물 2

HCID 10476Cyanogen BromideHCID 666077053-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,2-diamine

생성물 1

HCID 178422405HCID 178422405, 화합물수율 101.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,2-diamine (See Example 1.G) (500 mg, 2.015 mmol) and cyanic bromide (0.484 mL, 2.418 mmol) were added to a round bottom flask at room temperature, suspended in methanol (10.0 mL) and allowed to stir for 1.5 h. Volatiles were removed under reduced pressure followed by the addition of saturated sodium bicarbonate. The precipitate was collected via filtration, washed with ethyl acetate and dried under reduced pressure to afford the title compound (557 mg, 2.039 mmol, quant. yield). Compound was carried forward without further purification or characterization. MS (ESI) m/z 273.8 [M+1]+.

후처리

  1. customVolatiles were removed under reduced pressure
  2. additionfollowed by the addition of saturated sodium bicarbonate
  3. filtrationThe precipitate was collected via filtration
  4. washwashed with ethyl acetate
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-e65bb0a0166242aab1d4beccaa2991d2
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09193692B2

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