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Hydrochloric Acid → Diethyl-[4-(4-fluoro-phenyl)-6,7,8,9-tetrahydro-5H-pyrimido[4,5-c]azepin-2-yl]-amine

HRID 72796
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HRID 72796 반응식
C(OC([N:8]1[CH2:14][CH2:13][CH2:12][C:11]2[C:15]([C:24]3[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=3)=[N:16][C:17]([N:19]([CH2:22][CH3:23])[CH2:20][CH3:21])=[N:18][C:10]=2[CH2:9]1)=O)(C)(C)C.Cl>CCOC(C)=O.O1CCOCC1>[CH2:22]([N:19]([CH2:20][CH3:21])[C:17]1[N:16]=[C:15]([C:24]2[CH:25]=[CH:26][C:27]([F:30])=[CH:28][CH:29]=2)[C:11]2[CH2:12][CH2:13][CH2:14][NH:8][CH2:9][C:10]=2[N:18]=1)[CH3:23]
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 67369370HCID 67369370, 화합물

생성물 1

HCID 46205216Diethyl-[4-(4-fluoro-phenyl)-6,7,8,9-tetrahydro-5H-pyrimido[4,5-c]azepin-2-yl]-amine수율 90%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매

실험 절차

To a solution of 2-diethylamino-4-(4-fluoro-phenyl)-5,6,7,9-tetrahydro-pyrimido[4,5-c]azepine-8-carboxylic acid tert-butyl ester (0.058 g, 0.14 mmol) in EtOAc (1 mL) was added 4 M HCl in dioxane (2 mL). After 16 h, the mixture was concentrated, diluted with saturated (satd.) aqueous (aq.) NaHCO3, and extracted with CH2Cl2. The combined organic layers were dried and concentrated. Purification by FCC (2 M NH3 in MeOH/CH2Cl2) provided the title compound (>90%). HPLC: Rt=9.7 min. MS (ESI): mass calcd. for C18H23FN4, 314.4; m/z found, 315.4 [M+H]+. 1H NMR (CDCl3): 7.47 (dd, J=8.7, 5.5, 2H), 7.11 (t, J=8.7, 2H), 3.96 (5, 2H), 3.64 (q, J=7.0, 4H), 3.21-3.18 (m, 1H), 2.80-2.76 (m, 2H), 1.93-1.86 (m, 2H), 1.71-1.67 (m, 1H), 1.17 (t, J=7.0, 6H).

후처리

  1. concentrationthe mixture was concentrated
  2. additiondiluted with saturated (satd.) aqueous (aq.) NaHCO3
  3. extractionextracted with CH2Cl2
  4. customThe combined organic layers were dried
  5. concentrationconcentrated
  6. customPurification by FCC (2 M NH3 in MeOH/CH2Cl2)

출처 및 근거

ORD 기록
ord-6c17690f28564c4093fdae5dd8852028
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829011B2

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