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Methanesulfonyl chloride → HCID 59332855, 화합물

HRID 1879993
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반응식

HRID 1879993 반응식
[Br:1][C:2]1[CH:12]=[N:11][C:5]2[NH:6][CH2:7][CH2:8][NH:9][CH2:10][C:4]=2[CH:3]=1.[CH3:13][S:14](Cl)(=[O:16])=[O:15]>C(Cl)Cl>[Br:1][C:2]1[CH:12]=[N:11][C:5]2[NH:6][CH2:7][CH2:8][N:9]([S:14]([CH3:13])(=[O:16])=[O:15])[CH2:10][C:4]=2[CH:3]=1
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참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 59332834HCID 59332834, 화합물

생성물 1

HCID 59332855HCID 59332855, 화합물수율 48.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 7-bromo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepine (432 mg, 1.89 mmol) and TEA (0.28 mL, 2.02 mmol) in anhydrous CH2Cl2 (20 mL) under argon was added methanesulfonyl chloride (0.16 mL, 2.06 mmol). The mixture was stirred for 12 h at room temperature. Mixture was then concentrated to a brown solid and redissolved in a 2:1 MeOH:DMSO mixture. Purification by preparative HPLC (water/acetonitrile/0.05% TFA mixture) gave the title compound (7-bromo-4-(methylsulfonyl)-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepine) (281 mg, 48%) as a yellow solid: 1H NMR (200 MHz, DMSO-d6) δ 8.02 (s, 1H), 7.68 (s, 1H), 4.39 (s, 2H), 3.48 (s, 2H), 3.39 (s, 2H), 2.79 (s, 3H).

후처리

  1. concentrationMixture was then concentrated to a brown solid
  2. dissolutionredissolved in a 2:1 MeOH
  3. customPurification by preparative HPLC (water/acetonitrile/0.05% TFA mixture)

출처 및 근거

ORD 기록
ord-f4b1a7c039e54cbab8b2ece1261f9b31
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318720B2

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