Hydrochloric Acid → HCID 16659985, compound

HRID 1362329Notes

Reaction equation

HRID 1362329 reaction equation
[CH3:1][C:2]1([CH3:31])[C:8](=[O:9])[NH:7][C:6]2[N:10]=[CH:11][C:12](/[CH:14]=[CH:15]/[C:16]([N:18]([CH3:30])[CH2:19][C:20]3[N:21]([CH3:29])[C:22]4[C:27]([CH:28]=3)=[CH:26][CH:25]=[CH:24][CH:23]=4)=[O:17])=[CH:13][C:5]=2[CH2:4][NH:3]1.[ClH:32]>C(Cl)Cl.CCOCC>[ClH:32].[CH3:1][C:2]1([CH3:31])[C:8](=[O:9])[NH:7][C:6]2[N:10]=[CH:11][C:12](/[CH:14]=[CH:15]/[C:16]([N:18]([CH3:30])[CH2:19][C:20]3[N:21]([CH3:29])[C:22]4[C:27]([CH:28]=3)=[CH:26][CH:25]=[CH:24][CH:23]=4)=[O:17])=[CH:13][C:5]=2[CH2:4][NH:3]1

Participants

5

Procedure

A suspension of (E)-3-(3,3-dimethyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-7-yl)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)acrylamide (0.15 g, 0.36 mmol) in CH2Cl2 (5 mL) was treated with anhydrous HCl (0.36 mL of a 1.0 M solution in Et2O, 0.36 mmol). After stirring for 10 min, the mixture was diluted with Et2O (50 mL) and then stirred for 1.5 h. The solid was isolated by filtration, washed with Et2O, and dried under vacuum at 50° C. for 3 d to give the title compound (0.14 g, 83%) as a tan powder and as a mixture of amide rotamers: 1H NMR (500 MHz, DMSO-d6) δ 10.90-10.87 (m, 1H), 10.54 (br s, 2H), 8.66-8.63 (m, 1H), 8.39-8.33 (s, 1H), 7.62-7.59 (m, 1H), 7.51-7.32 (m, 3H), 7.14-7.11 (m, 1H), 7.03-6.99 (m, 1H), 6.43-6.19 (m, 1H), 5.07-4.86 (m, 2H), 4.40-4.35 (m, 2H), 3.74-3.69 (m, 3H), 3.13-3.00 (m, 3H), 1.63-1.59 (m, 6H); MS (ESI) n/e 418 (M+H)+.

Workup

  1. stirringstirred for 1.5 h
  2. customThe solid was isolated by filtration
  3. washwashed with Et2O
  4. customdried under vacuum at 50° C. for 3 d

Sources & evidence

ORD record
ord-e0d54553a5ee4653a6b8fd1c549070d4
Source dataset
uspto-grants-2011_02
Patent number
US07879872B2

Reaction notes

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