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Hydrochloric Acid → (S)-1-amino-3-methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one hydrochloride

HRID 2376625
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HRID 2376625 반응식
C(O)(=O)[C@@H](C1C=CC=CC=1)O.[NH2:12][C@H:13]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH2:17][CH2:16][N:15]([CH3:24])[C:14]1=[O:25].[ClH:26]>C(OCC)(=O)C>[ClH:26].[NH2:12][C@H:13]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH2:17][CH2:16][N:15]([CH3:24])[C:14]1=[O:25]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 131727233HCID 131727233, 화합물

생성물 1

HCID 44178389(S)-1-amino-3-methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one hydrochloride수율 92.5%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
50 °C

실험 절차

(S)-1-Amino-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepin-2-one (R)-mandelic acid salt (2.42 g, 7.06 mmol, 98.4% ee) was slurried in 25 mL ethyl acetate at ambient temperature. Concentrated aqueous hydrochloric acid (1.1 mL, about 11.2 mmol) was added and the mixture was heated to 50° C. with vigorous stirring for 3.5 hours. The slurry was cooled to ambient temperature and filtered, rinsed with the methyl t-butyl ether (about 10 mL) to give 1.48 g of the title compound (92.5% yield, 97.9% ee).

후처리

  1. temperatureThe slurry was cooled to ambient temperature
  2. filtrationfiltered
  3. washrinsed with the methyl t-butyl ether (about 10 mL)

출처 및 근거

ORD 기록
ord-cee1598c20e747b885863a5f4e025e71
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07468365B2

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