Hydrochloric Acid → HCID 58203940, compound

HRID 2385949Notes

Reaction equation

HRID 2385949 reaction equation
C(OC([N:8]1[CH2:11][CH:10]([NH:12][C:13]2[CH:14]=[CH:15][C:16]3[O:25][CH2:24][CH2:23][C:22]4[CH:21]=[C:20]([C:26]5[N:27]([C:31]6[CH:36]=[CH:35][C:34]([F:37])=[CH:33][C:32]=6[F:38])[N:28]=[CH:29][N:30]=5)[S:19][C:18]=4[C:17]=3[N:39]=2)[CH2:9]1)=O)(C)(C)C.Cl>CCOC(C)=O>[NH:8]1[CH2:11][CH:10]([NH:12][C:13]2[CH:14]=[CH:15][C:16]3[O:25][CH2:24][CH2:23][C:22]4[CH:21]=[C:20]([C:26]5[N:27]([C:31]6[CH:36]=[CH:35][C:34]([F:37])=[CH:33][C:32]=6[F:38])[N:28]=[CH:29][N:30]=5)[S:19][C:18]=4[C:17]=3[N:39]=2)[CH2:9]1

Participants

4

Procedure

3-{2-[2-(2,4-Difluoro-phenyl)-2H-[1,2,4]triazol-3-yl]-4,5-dihydro-6-oxa-1-thia-10-aza-benzo[e]azulen-9-ylamino}-azetidine-1-carboxylic acid tert-butyl ester (558 mg, 1.0 mmol) was dissolved in EtOAc (10 mL). Hydrogen chloride dissolved in Ethyl acetate (EtOAc—HCl, 10 mL) was added by drop to the solution and the reaction mixture was stirred at room temperature for 2 h. The reaction mixture was filtered to gather the solid which was washed with DCM (10 mL) to give 435 (0.43 g, yield: 87%). 1HNMR (DMSO-d6, 400 MHz): δ7.99 (s, 1H), 7.74-7.72 (m, 1H), 7.36-7.27 (m, 2H), 7.14 (s, 1H), 7.00 (d, J=8.8 Hz, 1H), 6.38-6.26 (m, 2H), 4.11-4.09 (m, 6H), 3.56 (s, 1H), 3.02 (t, J=4.8 Hz, 2H). ESI-MS: m/z=453 [M+H+]

Workup

  1. additionwas added by drop to the solution
  2. filtrationThe reaction mixture was filtered
  3. washwas washed with DCM (10 mL)

Sources & evidence

ORD record
ord-9cc73c3243f54bc9b8a17fa11a84b21f
Source dataset
uspto-grants-2012_09
Patent number
US08263633B2

Reaction notes

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