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Ammonia → 6-chloro-N-methyl-N-phenyl-[1,3,5]triazine-2,4-diamine

HRID 341473
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HRID 341473 반응식
Cl[C:2]1[N:7]=[C:6]([Cl:8])[N:5]=[C:4]([N:9]([CH3:16])[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:3]=1.[NH3:17]>C1COCC1>[Cl:8][C:6]1[N:5]=[C:4]([N:9]([CH3:16])[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:3]=[C:2]([NH2:17])[N:7]=1
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참가 물질

4

반응물 2

HCID 222Ammonia2회HCID 198964,6-dichloro-N-methyl-N-phenyl-1,3,5-triazin-2-amine2회

생성물 1

HCID 807666266-chloro-N-methyl-N-phenyl-[1,3,5]triazine-2,4-diamine수율 110%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a stirred solution of (4,6-dichloro-[1,3,5]triazin-2-yl)-methyl-phenyl-amine (Intermediate 42, 2.7 g, 10.58 mmol) in THF (45 ml) was added a solution of conc. aqueous ammonia (3 ml, 52.91 mmol). The reaction was allowed to stir at room temperature for 1 h, the reaction was then diluted with THF (50 ml), treated with conc. aqueous ammonia (1 ml, 17.64 mmol) and stirred for 18 h. The reaction was concentrated under vacuum and taken up in DCM (150 ml); the solution was then extracted with 2M aq. HCl (2×50 mL), and saturated brine (20 mL) and dried further over anhydrous sodium sulfate. The organic phase was evaporated to dryness to furnish the product as an off white solid (2.743 g, 110%). Method B HPLC-MS: MH+ requires m/z=236. Found: m/z=236, Rt=1.76 min (88%). 1H NMR (500 MHz, CDCl3) δ ppm 7.09-7.44 (5H, m), 5.21-5.65 (2H, m), 3.40 (3H, s).

후처리

  1. stirringstirred for 18 h
  2. concentrationThe reaction was concentrated under vacuum
  3. extractionthe solution was then extracted with 2M aq. HCl (2×50 mL), and saturated brine (20 mL)
  4. dry with materialdried further over anhydrous sodium sulfate
  5. customThe organic phase was evaporated to dryness

출처 및 근거

ORD 기록
ord-0e57402353de4b5abd7e9d122aec1bfd
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895733B2

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