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Hydrochloric Acid → 2-[2-[(4aR,7aR)-2-Amino-7a-isothiazol-5-yl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-6-yl]-5-fluoro-6-methyl-pyrimidin-4-yl]propan-2-ol hydrochloride

HRID 470295
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HRID 470295 반응식
[F:1][C:2]1[C:3]([C:32]([OH:35])([CH3:34])[CH3:33])=[N:4][C:5]([N:9]2[CH2:17][C@@H:16]3[C@@:11]([C:27]4[S:31][N:30]=[CH:29][CH:28]=4)([N:12]=[C:13]([NH:18]C(=O)C4C=CC=CC=4)[S:14][CH2:15]3)[CH2:10]2)=[N:6][C:7]=1[CH3:8].N1C=CC=CC=1.[ClH:42].CON.Cl.O1CCOCC1>C(O)C.C(Cl)Cl>[ClH:42].[NH2:18][C:13]1[S:14][CH2:15][C@@H:16]2[CH2:17][N:9]([C:5]3[N:4]=[C:3]([C:32]([OH:35])([CH3:34])[CH3:33])[C:2]([F:1])=[C:7]([CH3:8])[N:6]=3)[CH2:10][C@:11]2([C:27]2[S:31][N:30]=[CH:29][CH:28]=2)[N:12]=1
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8

반응물 5

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 312751,4-DioxaneHCID 521874O-Methylhydroxylamine hydrochlorideHCID 86762241N-[(4aR,7aR)-6-[5-Fluoro-4-(1-hydroxy-1-methyl-ethyl)-6-methyl-pyrimidin-2-yl]-7a-isothiazol-5-yl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide

생성물 1

HCID 86762256
2-[2-[(4aR,7aR)-2-Amino-7a-isothiazol-5-yl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-6-yl]-5-fluoro-6-methyl-pyrimidin-4-yl]propan-2-ol hydrochloride
수율 62.5%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6344Dichloromethane용매

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온도
70 °C

실험 절차

N-[(4aR,7aR)-6-[5-Fluoro-4-(1-hydroxy-1-methyl-ethyl)-6-methyl-pyrimidin-2-yl]-7a-isothiazol-5-yl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (33 mg, 0.064 mmol) is dissolved in ethanol (2 mL). To this solution is added pyridine (0.052 mL, 0.6 mmol) and O-methylhydroxylamine hydrochloride (55 mg, 0.6 mmol). The reaction is warmed to 70° C. for 4 hours. The reaction is cooled to room temperature and stirred overnight (˜16 hrs). The mixture is concentrated to give the crude product which is purified via silica gel chromatography using a 0-10% (7 N NH3 in MeOH)/DCM to give the pure freebase. The freebase is dissolved in DCM (2 mL) and treated with 4 M HCl in dioxane (0.3 mL, 1.2 mmol). The mixture is concentrated to give the title compound as a white solid (18 mg, 0.04 mmol). ES/MS (m/z): 409 (M+H). [α]D20=−6.0° (C=1.0, MeOH).

후처리

  1. temperatureThe reaction is cooled to room temperature
  2. concentrationThe mixture is concentrated
  3. customto give the crude product which
  4. customis purified via silica gel chromatography
  5. customto give the pure freebase
  6. concentrationThe mixture is concentrated

출처 및 근거

ORD 기록
ord-cd89b06d82c6459b8be55e0293dd9e8e
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08629270B2

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